Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67942967G= , CM000678.2:g.67942967G= | GRCh38 |
| NC_000016.9:g.67976870G= , CM000678.1:g.67976870G= | GRCh37 |
| NC_000016.8:g.66534371G= | NCBI36 |
| NG_009778.1:g.6146C= | |
| NG_033098.1:g.30728C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264005.10:c.321C= MANE Select | ENSP00000264005.5:p.Tyr107= | |
| ENST00000264005.9:c.321C= | ENSP00000264005.5:p.Tyr107= | |
| ENST00000570369.5:c.49C= | ||
| ENST00000570980.1:c.105C= | ENSP00000464651.1:p.Tyr35= | |
| ENST00000575277.1:n.99C= | ||
| ENST00000575467.5:c.*16C= | ENSP00000460653.1:n.*16C= | |
| NM_000229.1:c.321C= | NP_000220.1:p.Tyr107= | |
| NM_000229.2:c.321C= MANE Select | NP_000220.1:p.Tyr107= |