Linked Data
ClinVar Variation Id:
449254
dbSNP Id:
rs771619614
ExAC:
9:98003005 T / C
gnomAD v2:
9-98003005-T-C
gnomAD v3:
9-95240723-T-C
gnomAD v4:
9-95240723-T-C
COSMIC:
COSM1625274
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95240723T>C , CM000671.2:g.95240723T>C | GRCh38 |
| NC_000009.11:g.98003005T>C , CM000671.1:g.98003005T>C | GRCh37 |
| NC_000009.10:g.97042826T>C | NCBI36 |
| NG_011707.1:g.81987A>G , LRG_497:g.81987A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696261.1:n.517A>G | ||
| ENST00000696262.1:c.271A>G | ENSP00000512510.1:p.Ile91Val | |
| ENST00000289081.8:c.271A>G MANE Select | ENSP00000289081.3:p.Ile91Val | |
| ENST00000375305.6:c.271A>G | ENSP00000364454.1:p.Ile91Val | |
| ENST00000490972.7:c.271A>G | ENSP00000479931.1:p.Ile91Val | |
| ENST00000636777.1:n.329A>G | ||
| ENST00000647778.1:c.271A>G | ENSP00000498125.1:p.Ile91Val | |
| ENST00000647882.1:c.271A>G | ENSP00000497025.1:p.Ile91Val | |
| ENST00000648415.1:n.1909A>G | ||
| ENST00000649334.1:c.271A>G | ENSP00000497735.1:p.Ile91Val | |
| ENST00000649519.1:c.271A>G | ENSP00000497630.1:p.Ile91Val | |
| ENST00000649872.1:c.271A>G | ENSP00000497195.1:p.Ile91Val | |
| ENST00000650176.1:n.451A>G | ||
| ENST00000289081.7:c.271A>G | ENSP00000289081.3:p.Ile91Val | |
| ENST00000375305.5:c.271A>G | ENSP00000364454.1:p.Ile91Val | |
| ENST00000433829.1:c.271A>G | ENSP00000406908.1:p.Ile91Val | |
| ENST00000474949.1:n.533A>G | ||
| ENST00000490972.6:c.271A>G | ENSP00000479931.1:p.Ile91Val | |
| NM_000136.2:c.271A>G , LRG_497t1:c.271A>G | NP_000127.2:p.Ile91Val | |
| NM_001243743.1:c.271A>G | NP_001230672.1:p.Ile91Val | |
| NM_001243744.1:c.271A>G | NP_001230673.1:p.Ile91Val | |
| XM_006717001.1:c.271A>G | XP_006717064.1:p.Ile91Val | |
| XM_006717002.2:c.271A>G | XP_006717065.1:p.Ile91Val | |
| XM_006717004.2:c.271A>G | XP_006717067.1:p.Ile91Val | |
| XM_011518365.1:c.271A>G | XP_011516667.1:p.Ile91Val | |
| XM_011518366.1:c.271A>G | XP_011516668.1:p.Ile91Val | |
| XM_011518367.1:c.-331A>G | XP_011516669.1:n.-331A>G | |
| XM_006717001.3:c.271A>G | XP_006717064.1:p.Ile91Val | |
| XM_006717002.4:c.271A>G | XP_006717065.1:p.Ile91Val | |
| XM_006717004.4:c.271A>G | XP_006717067.1:p.Ile91Val | |
| XM_011518365.3:c.271A>G | XP_011516667.1:p.Ile91Val | |
| XM_011518366.3:c.271A>G | XP_011516668.1:p.Ile91Val | |
| XM_011518367.2:c.-331A>G | XP_011516669.1:n.-331A>G | |
| XM_017014452.2:c.-331A>G | XP_016869941.1:n.-331A>G | |
| XM_017014453.1:c.-331A>G | XP_016869942.1:n.-331A>G | |
| XM_017014454.1:c.-331A>G | XP_016869943.1:n.-331A>G | |
| XM_024447451.1:c.271A>G | XP_024303219.1:p.Ile91Val | |
| NM_000136.3:c.271A>G MANE Select | NP_000127.2:p.Ile91Val | |
| NM_001243743.2:c.271A>G | NP_001230672.1:p.Ile91Val | |
| NM_001243744.2:c.271A>G | NP_001230673.1:p.Ile91Val |