Linked Data
gnomAD v3:
6-31357175-A-C
gnomAD v4:
6-31357175-A-C
MyVariant Identifiers:
chr6:g.31324952A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31357175A>C , CM000668.2:g.31357175A>C | GRCh38 |
| NC_000006.11:g.31324952A>C , CM000668.1:g.31324952A>C | GRCh37 |
| NC_000006.10:g.31432931A>C | NCBI36 |
| NG_023187.1:g.5038T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.1457T>G | ||
| ENST00000481849.6:n.1457T>G | ||
| ENST00000497377.6:n.1457T>G | ||
| ENST00000696559.1:c.-17T>G | ENSP00000512717.1:n.-17T>G | |
| ENST00000696560.1:c.-17T>G | ENSP00000512718.1:n.-17T>G | |
| ENST00000696561.1:c.-17T>G | ENSP00000512719.1:n.-17T>G | |
| ENST00000696562.1:c.-17T>G | ENSP00000512720.1:n.-17T>G | |
| ENST00000412585.7:c.-17T>G MANE Select | ENSP00000399168.2:n.-17T>G | |
| ENST00000412585.6:c.-17T>G | ENSP00000399168.2:n.-17T>G | |
| ENST00000434333.1:c.-112T>G | ENSP00000405931.1:n.-112T>G | |
| ENST00000498007.1:n.5T>G | ||
| ENST00000603274.1:n.529A>C | ||
| NM_005514.6:c.-17T>G | NP_005505.2:n.-17T>G | |
| NM_005514.7:c.-17T>G | NP_005505.2:n.-17T>G | |
| NM_005514.8:c.-17T>G MANE Select | NP_005505.2:n.-17T>G |