Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186085775G= , CM000666.2:g.186085775G= | GRCh38 |
| NC_000004.11:g.187006929G= , CM000666.1:g.187006929G= | GRCh37 |
| NC_000004.10:g.187243923G= | NCBI36 |
| NG_007278.1:g.21621G= , LRG_117:g.21621G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698352.1:c.*3169G= | ENSP00000513675.1:n.*3169G= | |
| ENST00000698353.1:n.3492G= | ||
| ENST00000698354.1:c.*902G= | ENSP00000513676.1:n.*902G= | |
| ENST00000296795.8:c.*902G= MANE Select | ENSP00000296795.3:n.*902G= | |
| ENST00000296795.7:c.*902G= | ENSP00000296795.2:n.*902G= | |
| NM_003265.3:c.*902G= MANE Select | NP_003256.1:n.*902G= |