Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6718376G>A , CM000681.2:g.6718376G>A | GRCh38 |
| NC_000019.9:g.6718387G>A , CM000681.1:g.6718387G>A | GRCh37 |
| NC_000019.8:g.6669387G>A | NCBI36 |
| NG_009557.1:g.7276C>T , LRG_27:g.7276C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000594936.2:n.365C>T | ||
| ENST00000695652.1:c.181C>T | ENSP00000512083.1:p.Arg61Cys | |
| ENST00000695693.1:c.304C>T | ENSP00000512104.1:p.Arg102Cys | |
| ENST00000245907.11:c.304C>T MANE Select | ENSP00000245907.4:p.Arg102Cys | |
| ENST00000245907.10:c.304C>T | ENSP00000245907.4:p.Arg102Cys | |
| ENST00000594936.1:n.365C>T | ||
| ENST00000600744.1:c.181C>T | ENSP00000472044.1:p.Arg61Cys | |
| NM_000064.3:c.304C>T | NP_000055.2:p.Arg102Cys | |
| NM_000064.4:c.304C>T MANE Select | NP_000055.2:p.Arg102Cys |