Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67942967G>C , CM000678.2:g.67942967G>C | GRCh38 |
| NC_000016.9:g.67976870G>C , CM000678.1:g.67976870G>C | GRCh37 |
| NC_000016.8:g.66534371G>C | NCBI36 |
| NG_009778.1:g.6146C>G | |
| NG_033098.1:g.30728C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000229.2:c.321C>G MANE Select | NP_000220.1:p.Tyr107Ter |
| ENST00000264005.10:c.321C>G MANE Select | ENSP00000264005.5:p.Tyr107Ter |
| NM_000229.1:c.321C>G | NP_000220.1:p.Tyr107Ter |
| ENST00000264005.9:c.321C>G | ENSP00000264005.5:p.Tyr107Ter |
| ENST00000570369.5:c.49C>G | |
| ENST00000570980.1:c.105C>G | ENSP00000464651.1:p.Tyr35Ter |
| ENST00000575277.1:n.99C>G | |
| ENST00000575467.5:c.*16C>G | ENSP00000460653.1:n.*16C>G |