Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101425453C= , CM000671.2:g.101425453C= | GRCh38 |
| NC_000009.11:g.104187735C= , CM000671.1:g.104187735C= | GRCh37 |
| NC_000009.10:g.103227556C= | NCBI36 |
| NG_012387.1:g.15328G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647789.2:c.799G= MANE Select | ENSP00000497767.1:p.Gly267= | |
| ENST00000648064.1:c.799G= | ENSP00000497990.1:p.Gly267= | |
| ENST00000648758.1:c.799G= | ENSP00000497731.1:p.Gly267= | |
| ENST00000649902.1:c.799G= | ENSP00000497216.1:p.Gly267= | |
| ENST00000374855.8:c.799G= | ENSP00000363988.4:p.Gly267= | |
| ENST00000616752.1:c.799G= | ENSP00000481363.1:p.Gly267= | |
| NM_000035.3:c.799G= | NP_000026.2:p.Gly267= | |
| NM_000035.4:c.799G= MANE Select | NP_000026.2:p.Gly267= |