Linked Data
dbSNP Id:
rs1050341
ExAC:
6:31323337 T / C
gnomAD v2:
6-31323337-T-C
gnomAD v3:
6-31355560-T-C
gnomAD v4:
6-31355560-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31355560T>C , CM000668.2:g.31355560T>C | GRCh38 |
| NC_000006.11:g.31323337T>C , CM000668.1:g.31323337T>C | GRCh37 |
| NC_000006.10:g.31431316T>C | NCBI36 |
| NG_023187.1:g.6653A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000474381.2:n.2699A>G | ||
| ENST00000481849.6:n.2125A>G | ||
| ENST00000497377.6:n.2125A>G | ||
| ENST00000640094.2:c.652A>G | ENSP00000491275.2:p.Ile218Val | |
| ENST00000696558.1:c.721A>G | ENSP00000512716.1:n.721A>G | |
| ENST00000696559.1:c.652A>G | ENSP00000512717.1:p.Ile218Val | |
| ENST00000696560.1:c.652A>G | ENSP00000512718.1:p.Ile218Val | |
| ENST00000696561.1:c.652A>G | ENSP00000512719.1:p.Ile218Val | |
| ENST00000696562.1:c.652A>G | ENSP00000512720.1:p.Ile218Val | |
| ENST00000412585.7:c.652A>G MANE Select | ENSP00000399168.2:p.Ile218Val | |
| ENST00000412585.6:c.652A>G | ENSP00000399168.2:p.Ile218Val | |
| ENST00000434333.1:c.685A>G | ENSP00000405931.1:p.Ile229Val | |
| ENST00000463574.1:n.243A>G | ||
| ENST00000474381.1:n.1101A>G | ||
| ENST00000498007.1:n.918A>G | ||
| NM_005514.6:c.652A>G | NP_005505.2:p.Ile218Val | |
| XM_011514556.1:c.685A>G | XP_011512858.1:p.Ile229Val | |
| XM_011514557.1:c.652A>G | XP_011512859.1:p.Ile218Val | |
| XR_926175.1:n.1091A>G | ||
| NM_005514.7:c.652A>G | NP_005505.2:p.Ile218Val | |
| NM_005514.8:c.652A>G MANE Select | NP_005505.2:p.Ile218Val |