Linked Data
ClinVar Variation Id:
95691
ClinVar RCV Id:
RCV000081725
RCV000280063
RCV000547462
RCV000323400
RCV000372251
RCV002262625
RCV001271273
RCV004528293
dbSNP Id:
rs144313291
ExAC:
16:53674978 T / C
gnomAD v2:
16-53674978-T-C
gnomAD v3:
16-53641066-T-C
gnomAD v4:
16-53641066-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.53641066T>C , CM000678.2:g.53641066T>C | GRCh38 |
| NC_000016.9:g.53674978T>C , CM000678.1:g.53674978T>C | GRCh37 |
| NC_000016.8:g.52232479T>C | NCBI36 |
| NG_008991.2:g.67794A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262135.9:c.2925A>G | ENSP00000262135.4:p.Val975= | |
| ENST00000565343.2:n.3349A>G | ||
| ENST00000621565.5:c.2925A>G | ENSP00000480698.1:p.Val975= | |
| ENST00000647211.2:c.2925A>G MANE Select | ENSP00000493946.1:p.Val975= | |
| ENST00000680193.1:c.2925A>G | ENSP00000506379.1:p.Val975= | |
| ENST00000681587.1:n.937A>G | ||
| ENST00000262135.8:c.2925A>G | ENSP00000262135.4:p.Val975= | |
| ENST00000379925.7:c.2925A>G | ENSP00000369257.3:p.Val975= | |
| ENST00000563746.5:c.2925A>G | ENSP00000457889.1:p.Val975= | |
| ENST00000564374.5:c.2925A>G | ENSP00000456534.1:p.Val975= | |
| ENST00000621565.4:c.2925A>G | ENSP00000480698.1:p.Val975= | |
| NM_001127897.1:c.2925A>G | NP_001121369.1:p.Val975= | |
| NM_001127897.2:c.2925A>G | NP_001121369.1:p.Val975= | |
| NM_001308334.1:c.2925A>G | NP_001295263.1:p.Val975= | |
| NM_015272.2:c.2925A>G | NP_056087.2:p.Val975= | |
| NM_015272.3:c.2925A>G | NP_056087.2:p.Val975= | |
| XM_005255867.1:c.2925A>G | XP_005255924.1:p.Val975= | |
| XM_005255868.1:c.2937A>G | XP_005255925.1:p.Val979= | |
| XM_005255871.2:c.1170A>G | XP_005255928.1:p.Val390= | |
| XM_011522968.1:c.2925A>G | XP_011521270.1:p.Val975= | |
| XM_011522969.1:c.2937A>G | XP_011521271.1:p.Val979= | |
| XM_011522970.1:c.2937A>G | XP_011521272.1:p.Val979= | |
| XM_011522971.1:c.2937A>G | XP_011521273.1:p.Val979= | |
| XM_011522972.1:c.2937A>G | XP_011521274.1:p.Val979= | |
| XM_011522973.1:c.2937A>G | XP_011521275.1:p.Val979= | |
| XM_011522974.1:c.1170A>G | XP_011521276.1:p.Val390= | |
| XR_933260.1:n.2969A>G | ||
| NM_001127897.3:c.2925A>G | NP_001121369.1:p.Val975= | |
| NM_001308334.2:c.2925A>G | NP_001295263.1:p.Val975= | |
| NM_001330538.1:c.2925A>G | NP_001317467.1:p.Val975= | |
| NM_015272.4:c.2925A>G | NP_056087.2:p.Val975= | |
| XM_005255868.2:c.2937A>G | XP_005255925.1:p.Val979= | |
| XM_011522970.2:c.2937A>G | XP_011521272.1:p.Val979= | |
| XM_011522971.3:c.2937A>G | XP_011521273.1:p.Val979= | |
| XM_011522973.3:c.2937A>G | XP_011521275.1:p.Val979= | |
| XM_017023094.2:c.2937A>G | XP_016878583.1:p.Val979= | |
| XM_017023095.2:c.2937A>G | XP_016878584.1:p.Val979= | |
| XM_017023096.2:c.2937A>G | XP_016878585.1:p.Val979= | |
| XM_017023098.1:c.1170A>G | XP_016878587.1:p.Val390= | |
| XM_017023099.1:c.1170A>G | XP_016878588.1:p.Val390= | |
| XR_933260.3:n.2980A>G | ||
| NM_015272.5:c.2925A>G MANE Select | NP_056087.2:p.Val975= | |
| NM_001127897.4:c.2925A>G | NP_001121369.1:p.Val975= | |
| NM_001330538.2:c.2925A>G | NP_001317467.1:p.Val975= | |
| NM_001308334.3:c.2925A>G | NP_001295263.1:p.Val975= |