Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67942921G>A , CM000678.2:g.67942921G>A | GRCh38 |
| NC_000016.9:g.67976824G>A , CM000678.1:g.67976824G>A | GRCh37 |
| NC_000016.8:g.66534325G>A | NCBI36 |
| NG_009778.1:g.6192C>T | |
| NG_033098.1:g.30774C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000229.2:c.367C>T MANE Select | NP_000220.1:p.Arg123Cys |
| ENST00000264005.10:c.367C>T MANE Select | ENSP00000264005.5:p.Arg123Cys |
| NM_000229.1:c.367C>T | NP_000220.1:p.Arg123Cys |
| ENST00000264005.9:c.367C>T | ENSP00000264005.5:p.Arg123Cys |
| ENST00000570369.5:c.95C>T | |
| ENST00000570980.1:c.151C>T | ENSP00000464651.1:p.Arg51Cys |
| ENST00000573538.5:c.10C>T | ENSP00000463220.1:p.Arg4Cys |
| ENST00000575277.1:n.145C>T | |
| ENST00000575467.5:c.*62C>T | ENSP00000460653.1:n.*62C>T |