Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.106932812C= , CM000666.2:g.106932812C= | GRCh38 |
| NC_000004.11:g.107853969C= , CM000666.1:g.107853969C= | GRCh37 |
| NC_000004.10:g.108073418C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285311.8:c.223-6863G= MANE Select | ENSP00000285311.3:n.223-6863G= | |
| ENST00000285311.7:c.223-6863G= | ENSP00000285311.3:n.223-6863G= | |
| ENST00000510463.1:c.85-6863G= | ENSP00000423797.1:n.85-6863G= | |
| ENST00000510534.1:n.444-6863G= | ||
| ENST00000513208.5:c.-78-6863G= | ENSP00000421255.1:n.-78-6863G= | |
| NM_014421.2:c.223-6863G= | NP_055236.1:n.223-6863G= | |
| NM_014421.3:c.223-6863G= MANE Select | NP_055236.1:n.223-6863G= |