Linked Data
dbSNP Id:
rs151341255
gnomAD v2:
6-31324085-C-T
gnomAD v3:
6-31356308-C-T
gnomAD v4:
6-31356308-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31356308C>T , CM000668.2:g.31356308C>T | GRCh38 |
| NC_000006.11:g.31324085C>T , CM000668.1:g.31324085C>T | GRCh37 |
| NC_000006.10:g.31432064C>T | NCBI36 |
| NG_023187.1:g.5905G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000474381.2:n.1951G>A | ||
| ENST00000481849.6:n.1951G>A | ||
| ENST00000497377.6:n.1951G>A | ||
| ENST00000640094.2:c.478G>A | ENSP00000491275.2:p.Ala160Thr | |
| ENST00000696558.1:c.478G>A | ENSP00000512716.1:p.Ala160Thr | |
| ENST00000696559.1:c.478G>A | ENSP00000512717.1:p.Ala160Thr | |
| ENST00000696560.1:c.478G>A | ENSP00000512718.1:p.Ala160Thr | |
| ENST00000696561.1:c.478G>A | ENSP00000512719.1:p.Ala160Thr | |
| ENST00000696562.1:c.478G>A | ENSP00000512720.1:p.Ala160Thr | |
| ENST00000412585.7:c.478G>A MANE Select | ENSP00000399168.2:p.Ala160Thr | |
| ENST00000412585.6:c.478G>A | ENSP00000399168.2:p.Ala160Thr | |
| ENST00000434333.1:c.511G>A | ENSP00000405931.1:p.Ala171Thr | |
| ENST00000474381.1:n.353G>A | ||
| ENST00000498007.1:n.744G>A | ||
| NM_005514.6:c.478G>A | NP_005505.2:p.Ala160Thr | |
| XM_011514556.1:c.511G>A | XP_011512858.1:p.Ala171Thr | |
| XM_011514557.1:c.478G>A | XP_011512859.1:p.Ala160Thr | |
| XR_926175.1:n.488G>A | ||
| NM_005514.7:c.478G>A | NP_005505.2:p.Ala160Thr | |
| NM_005514.8:c.478G>A MANE Select | NP_005505.2:p.Ala160Thr |