Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10646017G>T , CM000682.2:g.10646017G>T | GRCh38 |
| NC_000020.10:g.10626665G>T , CM000682.1:g.10626665G>T | GRCh37 |
| NC_000020.9:g.10574665G>T | NCBI36 |
| NG_007496.1:g.33030C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.1953C>A MANE Select | NP_000205.1:p.Tyr651Ter |
| ENST00000254958.10:c.1953C>A MANE Select | ENSP00000254958.4:p.Tyr651Ter |
| NM_000214.2:c.1953C>A | NP_000205.1:p.Tyr651Ter |
| ENST00000254958.9:c.1953C>A | ENSP00000254958.4:p.Tyr651Ter |
| ENST00000423891.6:n.1819C>A | |
| ENST00000488480.2:n.350C>A | |
| ENST00000612857.1:n.442C>A | |
| ENST00000613518.1:c.302C>A | |
| ENST00000617965.2:n.2542C>A |