Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42698345G>A , CM000668.2:g.42698345G>A | GRCh38 |
| NC_000006.11:g.42666083G>A , CM000668.1:g.42666083G>A | GRCh37 |
| NC_000006.10:g.42774061G>A | NCBI36 |
| NG_009176.1:g.29276C>T | |
| NG_009176.2:g.29276C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.991C>T MANE Select | ENSP00000230381.5:p.Gln331Ter | |
| ENST00000230381.6:c.991C>T | ENSP00000230381.5:p.Gln331Ter | |
| NM_000322.4:c.991C>T | NP_000313.2:p.Gln331Ter | |
| XR_926295.3:n.1878C>T | ||
| NM_000322.5:c.991C>T MANE Select | NP_000313.2:p.Gln331Ter |