Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.16133226C= , CM000663.2:g.16133226C= | GRCh38 |
| NC_000001.10:g.16459721C= , CM000663.1:g.16459721C= | GRCh37 |
| NC_000001.9:g.16332308C= | NCBI36 |
| NG_021396.1:g.27862G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358432.8:c.2007G= MANE Select | ENSP00000351209.5:p.Gln669= | |
| ENST00000358432.7:c.2007G= | ENSP00000351209.5:p.Gln669= | |
| ENST00000462805.1:n.225G= | ||
| NM_004431.3:c.2007G= | NP_004422.2:p.Gln669= | |
| NM_001329090.1:c.1845G= | NP_001316019.1:p.Gln615= | |
| NM_004431.4:c.2007G= | NP_004422.2:p.Gln669= | |
| NM_004431.5:c.2007G= MANE Select | NP_004422.2:p.Gln669= | |
| NM_001329090.2:c.1845G= | NP_001316019.1:p.Gln615= |