Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.91111461C= , CM000674.2:g.91111461C= | GRCh38 |
| NC_000012.11:g.91505238C= , CM000674.1:g.91505238C= | GRCh37 |
| NC_000012.10:g.90029369C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266718.5:c.-85G= MANE Select | ENSP00000266718.4:n.-85G= | |
| ENST00000266718.4:c.-85G= | ENSP00000266718.4:n.-85G= | |
| ENST00000548071.1:n.26G= | ||
| NM_002345.3:c.-85G= | NP_002336.1:n.-85G= | |
| NM_002345.4:c.-85G= MANE Select | NP_002336.1:n.-85G= |