Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.144474371C>A , CM000670.2:g.144474371C>A | GRCh38 |
| NC_000008.10:g.145699754C>A , CM000670.1:g.145699754C>A | GRCh37 |
| NC_000008.9:g.145670562C>A | NCBI36 |
| NG_030003.1:g.6965G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003923.3:c.965G>T MANE Select | NP_003914.1:p.Gly322Val |
| ENST00000377317.5:c.965G>T MANE Select | ENSP00000366534.4:p.Gly322Val |
| NM_003923.2:c.965G>T | NP_003914.1:p.Gly322Val |
| ENST00000377317.4:c.965G>T | ENSP00000366534.4:p.Gly322Val |