Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.45913628C>T , CM000669.2:g.45913628C>T | GRCh38 |
| NC_000007.13:g.45953227C>T , CM000669.1:g.45953227C>T | GRCh37 |
| NC_000007.12:g.45919752C>T | NCBI36 |
| NG_011508.1:g.12645G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613132.5:c.*222G>A MANE Select | ENSP00000477772.2:n.*222G>A | |
| ENST00000381083.9:c.*222G>A | ENSP00000370473.4:n.*222G>A | |
| ENST00000275521.10:c.*222G>A | ENSP00000275521.5:n.*222G>A | |
| ENST00000381086.9:c.*222G>A | ENSP00000370476.4:n.*222G>A | |
| ENST00000613132.4:c.1035G>A | ENSP00000477772.1:n.1035G>A | |
| NM_000598.4:c.*222G>A | NP_000589.2:n.*222G>A | |
| NM_001013398.1:c.*222G>A | NP_001013416.1:n.*222G>A | |
| NM_001013398.2:c.*222G>A | NP_001013416.1:n.*222G>A | |
| NM_000598.5:c.*222G>A MANE Select | NP_000589.2:n.*222G>A |