Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046073G= , CM000667.2:g.136046073G= | GRCh38 |
| NC_000005.9:g.135381762G= , CM000667.1:g.135381762G= | GRCh37 |
| NC_000005.8:g.135409661G= | NCBI36 |
| NG_012646.1:g.22179G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.299-262G= MANE Select | ENSP00000416330.2:n.299-262G= | |
| ENST00000442011.6:c.299-262G= | ENSP00000416330.2:n.299-262G= | |
| ENST00000504185.5:n.456-262G= | ||
| ENST00000506699.5:n.364-262G= | ||
| ENST00000507018.5:c.216-262G= | ||
| ENST00000515433.1:n.329G= | ||
| NM_000358.2:c.299-262G= | NP_000349.1:n.299-262G= | |
| NM_000358.3:c.299-262G= MANE Select | NP_000349.1:n.299-262G= |