Linked Data
ClinVar Variation Id:
507735
ClinVar RCV Id:
RCV001697338
dbSNP Id:
rs199642821
ExAC:
X:110924433 G / A
gnomAD v2:
X-110924433-G-A
gnomAD v3:
X-111681205-G-A
gnomAD v4:
X-111681205-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.111681205G>A , CM000685.2:g.111681205G>A | GRCh38 |
| NC_000023.10:g.110924433G>A , CM000685.1:g.110924433G>A | GRCh37 |
| NC_000023.9:g.110811089G>A | NCBI36 |
| NG_016238.1:g.5088G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000623622.2:c.-14G>A | ENSP00000485624.2:n.-14G>A | |
| ENST00000699748.1:c.-14G>A | ENSP00000514558.1:n.-14G>A | |
| ENST00000394780.8:c.-14G>A MANE Select | ENSP00000378260.3:n.-14G>A | |
| ENST00000636363.1:c.-14G>A | ENSP00000490681.1:n.-14G>A | |
| ENST00000251943.8:c.-451G>A | ENSP00000251943.4:n.-451G>A | |
| ENST00000371979.7:c.-14G>A | ENSP00000361047.3:n.-14G>A | |
| ENST00000394780.7:c.-14G>A | ENSP00000378260.3:n.-14G>A | |
| ENST00000468657.5:c.-14G>A | ENSP00000480638.2:n.-14G>A | |
| ENST00000473389.5:c.-14G>A | ENSP00000480711.1:n.-14G>A | |
| ENST00000482374.5:c.-14G>A | ENSP00000479632.1:n.-14G>A | |
| ENST00000486353.5:c.-14G>A | ENSP00000426892.2:n.-14G>A | |
| ENST00000487141.5:c.118-927G>A | ENSP00000478130.1:n.118-927G>A | |
| ENST00000492038.5:c.-14G>A | ENSP00000479483.1:n.-14G>A | |
| ENST00000495283.5:c.-14G>A | ENSP00000427093.3:n.-14G>A | |
| ENST00000610588.4:c.-314G>A | ENSP00000479731.1:n.-314G>A | |
| ENST00000621367.4:c.-347G>A | ENSP00000481509.1:n.-347G>A | |
| ENST00000622986.3:c.-14G>A | ENSP00000485067.1:n.-14G>A | |
| ENST00000622997.3:c.-14G>A | ENSP00000485420.1:n.-14G>A | |
| ENST00000623144.3:c.-14G>A | ENSP00000485279.1:n.-14G>A | |
| ENST00000624161.3:c.-14G>A | ENSP00000485181.1:n.-14G>A | |
| ENST00000624881.3:c.-14G>A | ENSP00000485093.1:n.-14G>A | |
| NM_001039210.3:c.-14G>A | NP_001034299.3:n.-14G>A | |
| NM_001099922.2:c.-14G>A | NP_001093392.1:n.-14G>A | |
| NM_001168385.1:c.-14G>A | NP_001161857.1:n.-14G>A | |
| NM_001257230.1:c.-222G>A | NP_001244159.1:n.-222G>A | |
| NM_001257231.1:c.-314G>A | NP_001244160.1:n.-314G>A | |
| NM_001257234.1:c.-347G>A | NP_001244163.1:n.-347G>A | |
| NM_001257235.1:c.-347G>A | NP_001244164.1:n.-347G>A | |
| NM_001257237.1:c.-451G>A | NP_001244166.1:n.-451G>A | |
| NM_001257240.1:c.-451G>A | NP_001244169.1:n.-451G>A | |
| NM_001257241.1:c.-314G>A | NP_001244170.1:n.-314G>A | |
| NM_018466.4:c.-14G>A | NP_060936.1:n.-14G>A | |
| NR_033125.1:n.88G>A | ||
| XM_006724693.2:c.-14G>A | XP_006724756.1:n.-14G>A | |
| XM_006724695.2:c.-14G>A | XP_006724758.1:n.-14G>A | |
| XM_006724697.2:c.-222G>A | XP_006724760.2:n.-222G>A | |
| XM_006724698.2:c.-347G>A | XP_006724761.2:n.-347G>A | |
| XM_011531028.1:c.-14G>A | XP_011529330.1:n.-14G>A | |
| XM_011531029.1:c.-14G>A | XP_011529331.1:n.-14G>A | |
| XM_011531030.1:c.-14G>A | XP_011529332.1:n.-14G>A | |
| XM_011531031.1:c.-451G>A | XP_011529333.1:n.-451G>A | |
| XR_938409.1:n.460G>A | ||
| NM_001039210.4:c.-14G>A | NP_001034299.3:n.-14G>A | |
| NM_001168385.2:c.-14G>A | NP_001161857.1:n.-14G>A | |
| NM_001257235.2:c.-347G>A | NP_001244164.1:n.-347G>A | |
| NM_001257240.2:c.-451G>A | NP_001244169.1:n.-451G>A | |
| NM_001257241.2:c.-314G>A | NP_001244170.1:n.-314G>A | |
| NM_001324290.1:c.-14G>A | NP_001311219.1:n.-14G>A | |
| NM_001324291.1:c.-222G>A | NP_001311220.1:n.-222G>A | |
| NM_001324292.1:c.-14G>A | NP_001311221.1:n.-14G>A | |
| NM_001324293.1:c.-451G>A | NP_001311222.1:n.-451G>A | |
| NM_018466.5:c.-14G>A | NP_060936.1:n.-14G>A | |
| NR_033125.2:n.88G>A | ||
| NR_136735.1:n.36G>A | ||
| NR_148693.1:n.88G>A | ||
| XM_006724693.3:c.-14G>A | XP_006724756.1:n.-14G>A | |
| XM_006724697.3:c.-222G>A | XP_006724760.2:n.-222G>A | |
| XM_006724698.3:c.-347G>A | XP_006724761.2:n.-347G>A | |
| XM_011531028.2:c.-14G>A | XP_011529330.1:n.-14G>A | |
| XM_011531030.2:c.-14G>A | XP_011529332.1:n.-14G>A | |
| XM_017029846.1:c.-14G>A | XP_016885335.1:n.-14G>A | |
| XM_017029847.1:c.-14G>A | XP_016885336.1:n.-14G>A | |
| XM_017029848.1:c.-14G>A | XP_016885337.1:n.-14G>A | |
| XM_017029849.1:c.-14G>A | XP_016885338.1:n.-14G>A | |
| XM_017029850.2:c.-14G>A | XP_016885339.1:n.-14G>A | |
| XM_017029851.1:c.-724G>A | XP_016885340.1:n.-724G>A | |
| XM_024452449.1:c.-14G>A | XP_024308217.1:n.-14G>A | |
| XR_001755726.1:n.27G>A | ||
| XR_001755727.1:n.27G>A | ||
| XR_001755728.1:n.27G>A | ||
| NM_001039210.5:c.-14G>A | NP_001034299.3:n.-14G>A | |
| NM_001099922.3:c.-14G>A MANE Select | NP_001093392.1:n.-14G>A | |
| NM_001168385.3:c.-14G>A | NP_001161857.1:n.-14G>A | |
| NM_001257230.2:c.-222G>A | NP_001244159.1:n.-222G>A | |
| NM_001257235.3:c.-347G>A | NP_001244164.1:n.-347G>A | |
| NM_001257240.3:c.-451G>A | NP_001244169.1:n.-451G>A | |
| NM_001257241.3:c.-314G>A | NP_001244170.1:n.-314G>A | |
| NM_001324290.2:c.-14G>A | NP_001311219.1:n.-14G>A | |
| NM_001324291.2:c.-222G>A | NP_001311220.1:n.-222G>A | |
| NM_001324292.2:c.-14G>A | NP_001311221.1:n.-14G>A | |
| NM_018466.6:c.-14G>A | NP_060936.1:n.-14G>A | |
| NR_033125.3:n.36G>A | ||
| NR_136735.2:n.36G>A | ||
| NR_148693.2:n.36G>A | ||
| NM_001257231.2:c.-314G>A | NP_001244160.1:n.-314G>A | |
| NM_001257234.2:c.-347G>A | NP_001244163.1:n.-347G>A | |
| NM_001257237.2:c.-451G>A | NP_001244166.1:n.-451G>A |