Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.97855197G= , CM000671.2:g.97855197G= | GRCh38 |
| NC_000009.11:g.100617479G= , CM000671.1:g.100617479G= | GRCh37 |
| NC_000009.10:g.99657300G= | NCBI36 |
| NG_011979.1:g.6943G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004473.4:c.*161G= MANE Select | NP_004464.2:n.*161G= |
| ENST00000375123.5:c.*161G= MANE Select | ENSP00000364265.3:n.*161G= |
| NM_004473.3:c.*161G= | NP_004464.2:n.*161G= |
| ENST00000375123.4:c.*161G= | ENSP00000364265.3:n.*161G= |