Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.170283328C>T , CM000668.2:g.170283328C>T | GRCh38 |
| NC_000006.11:g.170592416C>T , CM000668.1:g.170592416C>T | GRCh37 |
| NC_000006.10:g.170434341C>T | NCBI36 |
| NG_027940.1:g.12282G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005618.4:c.1951G>A MANE Select | NP_005609.3:p.Asp651Asn |
| ENST00000366756.4:c.1951G>A MANE Select | ENSP00000355718.3:p.Asp651Asn |
| NM_005618.3:c.1951G>A | NP_005609.3:p.Asp651Asn |
| ENST00000366756.3:c.1951G>A | ENSP00000355718.3:p.Asp651Asn |
| XM_005266934.2:c.1452-223G>A | XP_005266991.1:n.1452-223G>A |
| XM_005266934.4:c.1452-223G>A | XP_005266991.1:n.1452-223G>A |
| XM_011535758.1:c.1951G>A | XP_011534060.1:p.Asp651Asn |