Linked Data
dbSNP Id:
rs1051488
ExAC:
6:31322911 C / T
gnomAD v2:
6-31322911-C-T
gnomAD v3:
6-31355134-C-T
gnomAD v4:
6-31355134-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31355134C>T , CM000668.2:g.31355134C>T | GRCh38 |
| NC_000006.11:g.31322911C>T , CM000668.1:g.31322911C>T | GRCh37 |
| NC_000006.10:g.31430890C>T | NCBI36 |
| NG_023187.1:g.7079G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000474381.2:n.3032G>A | ||
| ENST00000481849.6:n.2551G>A | ||
| ENST00000497377.6:n.2458G>A | ||
| ENST00000640094.2:c.895+183G>A | ENSP00000491275.2:n.895+183G>A | |
| ENST00000696558.1:c.1054G>A | ENSP00000512716.1:n.1054G>A | |
| ENST00000696559.1:c.985G>A | ENSP00000512717.1:p.Ala329Thr | |
| ENST00000696560.1:c.985G>A | ENSP00000512718.1:p.Ala329Thr | |
| ENST00000696561.1:c.985G>A | ENSP00000512719.1:p.Ala329Thr | |
| ENST00000696562.1:c.985G>A | ENSP00000512720.1:p.Ala329Thr | |
| ENST00000412585.7:c.985G>A MANE Select | ENSP00000399168.2:p.Ala329Thr | |
| ENST00000640094.1:c.88+183G>A | ENSP00000491275.1:n.88+183G>A | |
| ENST00000412585.6:c.985G>A | ENSP00000399168.2:p.Ala329Thr | |
| ENST00000463574.1:n.576G>A | ||
| NM_005514.6:c.985G>A | NP_005505.2:p.Ala329Thr | |
| XM_011514556.1:c.1018G>A | XP_011512858.1:p.Ala340Thr | |
| XM_011514557.1:c.895+183G>A | XP_011512859.1:n.895+183G>A | |
| XR_926175.1:n.1424G>A | ||
| NM_005514.7:c.985G>A | NP_005505.2:p.Ala329Thr | |
| NM_005514.8:c.985G>A MANE Select | NP_005505.2:p.Ala329Thr |