Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10645993C>T , CM000682.2:g.10645993C>T | GRCh38 |
| NC_000020.10:g.10626641C>T , CM000682.1:g.10626641C>T | GRCh37 |
| NC_000020.9:g.10574641C>T | NCBI36 |
| NG_007496.1:g.33054G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000214.3:c.1977G>A MANE Select | NP_000205.1:p.Trp659Ter |
| ENST00000254958.10:c.1977G>A MANE Select | ENSP00000254958.4:p.Trp659Ter |
| NM_000214.2:c.1977G>A | NP_000205.1:p.Trp659Ter |
| ENST00000254958.9:c.1977G>A | ENSP00000254958.4:p.Trp659Ter |
| ENST00000423891.6:n.1843G>A | |
| ENST00000488480.2:n.374G>A | |
| ENST00000612857.1:n.466G>A | |
| ENST00000613518.1:c.326G>A | |
| ENST00000617965.2:n.2566G>A |