Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56044028G= , CM000674.2:g.56044028G= | GRCh38 |
| NC_000012.11:g.56437812G= , CM000674.1:g.56437812G= | GRCh37 |
| NC_000012.10:g.54724079G= | NCBI36 |
| NG_023201.1:g.7127G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001029.5:c.313-91G= MANE Select | NP_001020.2:n.313-91G= |
| ENST00000646449.2:c.313-91G= MANE Select | ENSP00000496643.1:n.313-91G= |
| NM_001029.3:c.313-91G= | NP_001020.2:n.313-91G= |
| ENST00000356464.10:c.313-91G= | ENSP00000348849.5:n.313-91G= |
| ENST00000356464.9:c.313-91G= | ENSP00000348849.5:n.313-91G= |
| ENST00000548590.1:n.1100-91G= | |
| ENST00000552361.1:c.313-91G= | ENSP00000450339.1:n.313-91G= |