Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.25206920G= , CM000684.2:g.25206920G= | GRCh38 |
| NC_000022.10:g.25602887G= , CM000684.1:g.25602887G= | GRCh37 |
| NC_000022.9:g.23932887G= | NCBI36 |
| NG_009828.1:g.12063G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004076.5:c.471-127G= MANE Select | NP_004067.1:n.471-127G= |
| ENST00000215855.7:c.471-127G= MANE Select | ENSP00000215855.2:n.471-127G= |
| NM_004076.4:c.471-127G= | NP_004067.1:n.471-127G= |
| ENST00000215855.6:c.471-127G= | ENSP00000215855.2:n.471-127G= |
| ENST00000404334.1:c.328-127G= | ENSP00000386123.1:n.328-127G= |
| XM_011529902.1:c.639-127G= | XP_011528204.1:n.639-127G= |
| XM_011529902.3:c.639-127G= | XP_011528204.1:n.639-127G= |
| XM_017028599.2:c.496-127G= | XP_016884088.1:n.496-127G= |