Linked Data
ClinVar Variation Id:
125803
dbSNP Id:
rs80358090
ExAC:
17:41209170 C / A
gnomAD v2:
17-41209170-C-A
gnomAD v3:
17-43057153-C-A
gnomAD v4:
17-43057153-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43057153C>A , CM000679.2:g.43057153C>A | GRCh38 |
| NC_000017.10:g.41209170C>A , CM000679.1:g.41209170C>A | GRCh37 |
| NC_000017.9:g.38462696C>A | NCBI36 |
| NG_005905.2:g.160831G>T , LRG_292:g.160831G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000461574.2:c.5191-18G>T | ENSP00000417241.2:n.5191-18G>T | |
| ENST00000470026.6:c.5194-18G>T | ENSP00000419274.2:n.5194-18G>T | |
| ENST00000473961.6:c.5068-18G>T | ENSP00000420201.2:n.5068-18G>T | |
| ENST00000476777.6:c.5188-18G>T | ENSP00000417554.2:n.5188-18G>T | |
| ENST00000477152.6:c.5116-18G>T | ENSP00000419988.2:n.5116-18G>T | |
| ENST00000478531.6:c.1882-18G>T | ENSP00000420412.2:n.1882-18G>T | |
| ENST00000489037.2:c.5116-18G>T | ENSP00000420781.2:n.5116-18G>T | |
| ENST00000493919.6:c.1744-18G>T | ENSP00000418819.2:n.1744-18G>T | |
| ENST00000494123.6:c.5194-18G>T | ENSP00000419103.2:n.5194-18G>T | |
| ENST00000497488.2:c.4306-18G>T | ENSP00000418986.2:n.4306-18G>T | |
| ENST00000618469.2:c.5194-18G>T | ENSP00000478114.2:n.5194-18G>T | |
| ENST00000634433.2:c.5071-18G>T | ENSP00000489431.2:n.5071-18G>T | |
| ENST00000644379.2:c.5260-18G>T | ENSP00000496570.2:n.5260-18G>T | |
| ENST00000644555.2:c.1744-18G>T | ENSP00000494614.2:n.1744-18G>T | |
| ENST00000652672.2:c.5053-18G>T | ENSP00000498906.2:n.5053-18G>T | |
| ENST00000484087.6:c.1756-18G>T | ENSP00000419481.2:n.1756-18G>T | |
| ENST00000357654.9:c.5194-18G>T MANE Select | ENSP00000350283.3:n.5194-18G>T | |
| ENST00000471181.7:c.5257-18G>T | ENSP00000418960.2:n.5257-18G>T | |
| ENST00000644379.1:c.1581-18G>T | ||
| ENST00000352993.7:c.1768-18G>T | ENSP00000312236.5:n.1768-18G>T | |
| ENST00000357654.7:c.5194-18G>T | ENSP00000350283.3:n.5194-18G>T | |
| ENST00000461221.5:c.*4977-18G>T | ENSP00000418548.1:n.*4977-18G>T | |
| ENST00000468300.5:c.1882-18G>T | ENSP00000417148.1:n.1882-18G>T | |
| ENST00000471181.6:c.5257-18G>T | ENSP00000418960.2:n.5257-18G>T | |
| ENST00000491747.6:c.1882-18G>T | ENSP00000420705.2:n.1882-18G>T | |
| ENST00000493795.5:c.5053-18G>T | ENSP00000418775.1:n.5053-18G>T | |
| ENST00000586385.5:c.124-18G>T | ENSP00000465818.1:n.124-18G>T | |
| ENST00000591534.5:c.667-18G>T | ENSP00000467329.1:n.667-18G>T | |
| ENST00000591849.5:c.-98-6963G>T | ENSP00000465347.1:n.-98-6963G>T | |
| NM_007294.3:c.5194-18G>T , LRG_292t1:c.5194-18G>T | NP_009225.1:n.5194-18G>T | |
| NM_007297.3:c.5053-18G>T | NP_009228.2:n.5053-18G>T | |
| NM_007298.3:c.1882-18G>T | NP_009229.2:n.1882-18G>T | |
| NM_007299.3:c.1882-18G>T | NP_009230.2:n.1882-18G>T | |
| NM_007300.3:c.5257-18G>T | NP_009231.2:n.5257-18G>T | |
| NR_027676.1:n.5330-18G>T | ||
| NM_007294.4:c.5194-18G>T MANE Select | NP_009225.1:n.5194-18G>T | |
| NM_007297.4:c.5053-18G>T | NP_009228.2:n.5053-18G>T | |
| NM_007299.4:c.1882-18G>T | NP_009230.2:n.1882-18G>T | |
| NM_007300.4:c.5257-18G>T | NP_009231.2:n.5257-18G>T | |
| NR_027676.2:n.5371-18G>T |