Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35500142C= , CM000668.2:g.35500142C= | GRCh38 |
| NC_000006.11:g.35467919C= , CM000668.1:g.35467919C= | GRCh37 |
| NC_000006.10:g.35575897C= | NCBI36 |
| NG_009077.1:g.17729G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229771.11:c.1334G= MANE Select | ENSP00000229771.6:p.Gly445= | |
| ENST00000229771.10:c.1334G= | ENSP00000229771.6:p.Gly445= | |
| ENST00000322263.8:c.1175G= | ENSP00000319414.4:p.Gly392= | |
| ENST00000495781.1:n.510G= | ||
| ENST00000614066.4:c.1328G= | ENSP00000477534.1:p.Gly443= | |
| NM_001289395.1:c.1175G= | NP_001276324.1:p.Gly392= | |
| NM_003322.4:c.1334G= | NP_003313.3:p.Gly445= | |
| NM_003322.5:c.1334G= | NP_003313.3:p.Gly445= | |
| NM_003322.6:c.1334G= MANE Select | NP_003313.3:p.Gly445= | |
| NM_001289395.2:c.1175G= | NP_001276324.1:p.Gly392= |