Linked Data
dbSNP Id:
rs200966417
ExAC:
6:10530065 T / A
gnomAD v2:
6-10530065-T-A
gnomAD v3:
6-10529832-T-A
gnomAD v4:
6-10529832-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.10529832T>A , CM000668.2:g.10529832T>A | GRCh38 |
| NC_000006.11:g.10530065T>A , CM000668.1:g.10530065T>A | GRCh37 |
| NC_000006.10:g.10638051T>A | NCBI36 |
| NG_007469.3:g.42610T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397423.7:n.484+991T>A | ||
| ENST00000495262.7:c.921T>A MANE Select | ENSP00000419411.2:p.Ile307= | |
| ENST00000379597.7:c.921T>A | ENSP00000368917.3:p.Ile307= | |
| ENST00000397423.6:n.484+991T>A | ||
| ENST00000410107.5:c.67+20674T>A | ENSP00000386321.1:n.67+20674T>A | |
| ENST00000461400.1:n.21T>A | ||
| ENST00000474518.1:n.508+991T>A | ||
| ENST00000474983.5:n.1498T>A | ||
| ENST00000475577.5:n.254+2172T>A | ||
| ENST00000483204.1:n.1497T>A | ||
| ENST00000485764.1:n.36T>A | ||
| ENST00000489225.5:n.283+36901T>A | ||
| ENST00000489819.5:n.175+8238T>A | ||
| ENST00000495262.5:c.921T>A | ENSP00000419411.1:p.Ile307= | |
| NM_145649.4:c.921T>A | NP_663624.1:p.Ile307= | |
| XM_005248999.2:c.690T>A | XP_005249056.1:p.Ile230= | |
| XM_006715052.2:c.921T>A | XP_006715115.1:p.Ile307= | |
| XM_006715053.2:c.921T>A | XP_006715116.1:p.Ile307= | |
| XM_011514465.1:c.921T>A | XP_011512767.1:p.Ile307= | |
| XM_011514467.1:c.690T>A | XP_011512769.1:p.Ile230= | |
| XM_011514468.1:c.921T>A | XP_011512770.1:p.Ile307= | |
| XR_926136.1:n.1472T>A | ||
| XM_006715052.3:c.921T>A | XP_006715115.1:p.Ile307= | |
| XM_011514468.3:c.921T>A | XP_011512770.1:p.Ile307= | |
| XM_017010732.2:c.921T>A | XP_016866221.1:p.Ile307= | |
| XR_002956275.1:n.1472T>A | ||
| XR_926136.2:n.1470T>A | ||
| NM_001374747.1:c.921T>A | NP_001361676.1:p.Ile307= | |
| NM_145649.5:c.921T>A MANE Select | NP_663624.1:p.Ile307= |