Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5993972C>T , CM000674.2:g.5993972C>T | GRCh38 |
| NC_000012.11:g.6103138C>T , CM000674.1:g.6103138C>T | GRCh37 |
| NC_000012.10:g.5973399C>T | NCBI36 |
| NG_009072.1:g.135699G>A | |
| NG_009072.2:g.135699G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000552.5:c.6488G>A MANE Select | NP_000543.3:p.Cys2163Tyr |
| ENST00000261405.10:c.6488G>A MANE Select | ENSP00000261405.5:p.Cys2163Tyr |
| NM_000552.3:c.6488G>A | NP_000543.2:p.Cys2163Tyr |
| NM_000552.4:c.6488G>A | NP_000543.2:p.Cys2163Tyr |
| ENST00000261405.9:c.6488G>A | ENSP00000261405.5:p.Cys2163Tyr |
| ENST00000538635.5:n.421-38G>A |