Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713482T= , CM000681.2:g.6713482T= | GRCh38 |
| NC_000019.9:g.6713493T= , CM000681.1:g.6713493T= | GRCh37 |
| NC_000019.8:g.6664493T= | NCBI36 |
| NG_009557.1:g.12170A= , LRG_27:g.12170A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.678A= | ENSP00000512083.1:p.Gly226= | |
| ENST00000695692.1:n.125A= | ||
| ENST00000245907.11:c.801A= MANE Select | ENSP00000245907.4:p.Gly267= | |
| ENST00000245907.10:c.801A= | ENSP00000245907.4:p.Gly267= | |
| ENST00000595577.1:n.305A= | ||
| ENST00000597442.5:n.51A= | ||
| NM_000064.3:c.801A= | NP_000055.2:p.Gly267= | |
| NM_000064.4:c.801A= MANE Select | NP_000055.2:p.Gly267= |