Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38144234C>G , CM000670.2:g.38144234C>G | GRCh38 |
| NC_000008.10:g.38001752C>G , CM000670.1:g.38001752C>G | GRCh37 |
| NC_000008.9:g.38120909C>G | NCBI36 |
| NG_011827.1:g.11849G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.*39G>C MANE Select | ENSP00000276449.3:n.*39G>C | |
| ENST00000276449.8:c.*39G>C | ENSP00000276449.3:n.*39G>C | |
| ENST00000520114.1:n.2866G>C | ||
| ENST00000522050.1:c.739G>C | ||
| NM_000349.2:c.*39G>C | NP_000340.2:n.*39G>C | |
| XM_006716392.1:c.803G>C | XP_006716455.1:p.Trp268Ser | |
| NM_000349.3:c.*39G>C MANE Select | NP_000340.2:n.*39G>C |