Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.143531263C= , CM000665.2:g.143531263C= | GRCh38 |
| NC_000003.11:g.143250105C= , CM000665.1:g.143250105C= | GRCh37 |
| NC_000003.10:g.144732795C= | NCBI36 |
| NG_017077.1:g.322269G= | |
| NG_017077.2:g.322269G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000316549.11:c.1089+21099G= MANE Select | ENSP00000320246.6:n.1089+21099G= | |
| ENST00000316549.10:c.1089+21099G= | ENSP00000320246.6:n.1089+21099G= | |
| NM_173653.3:c.1089+21099G= | NP_775924.1:n.1089+21099G= | |
| XM_011512703.1:c.441+21099G= | XP_011511005.1:n.441+21099G= | |
| XM_011512703.3:c.441+21099G= | XP_011511005.1:n.441+21099G= | |
| XM_017006202.2:c.1089+21099G= | XP_016861691.1:n.1089+21099G= | |
| XM_017006203.1:c.738+21099G= | XP_016861692.1:n.738+21099G= | |
| NM_173653.4:c.1089+21099G= MANE Select | NP_775924.1:n.1089+21099G= |