Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.117263062C>A , CM000672.2:g.117263062C>A | GRCh38 |
| NC_000010.10:g.119022573C>A , CM000672.1:g.119022573C>A | GRCh37 |
| NC_000010.9:g.119012563C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NM_003054.4:c.992-3671C>A VV | NP_003045.2:p.= | |
| NM_003054.5:c.992-3671C>A VV | NP_003045.2:p.= | |
| NM_003054.6:c.992-3671C>A VV MANE Preferred | NP_003045.2:p.= | |
| ENST00000298472.9:c.992-3671C>A | ENSP00000298472.5:p.= | |
| ENST00000497497.1:n.1408-3671C>A |