Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.98585634G= , CM000665.2:g.98585634G= | GRCh38 |
| NC_000003.11:g.98304478G= , CM000665.1:g.98304478G= | GRCh37 |
| NC_000003.10:g.99787168G= | NCBI36 |
| NG_015994.1:g.12978C= | |
| NG_015994.2:g.12978C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647941.2:c.979C= MANE Select | ENSP00000497326.1:p.His327= | |
| ENST00000264193.2:c.979C= | ENSP00000264193.2:p.His327= | |
| ENST00000510489.1:n.229C= | ||
| NM_000097.5:c.979C= | NP_000088.3:p.His327= | |
| XM_005247125.3:c.979C= | XP_005247182.1:p.His327= | |
| NM_000097.7:c.979C= MANE Select | NP_000088.3:p.His327= | |
| XM_005247125.4:c.979C= | XP_005247182.1:p.His327= | |
| XR_001740025.2:n.1150C= | ||
| XR_001740026.1:n.1714C= | ||
| XR_001740027.1:n.1254C= | ||
| XR_001740028.1:n.1220C= |