Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218814830G>A , CM000664.2:g.218814830G>A | GRCh38 |
| NC_000002.11:g.219679553G>A , CM000664.1:g.219679553G>A | GRCh37 |
| NC_000002.10:g.219387797G>A | NCBI36 |
| NG_007959.1:g.38082G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.1476+73G>A MANE Select | ENSP00000258415.4:n.1476+73G>A | |
| ENST00000258415.8:c.1476+73G>A | ENSP00000258415.4:n.1476+73G>A | |
| ENST00000494263.5:n.2188+73G>A | ||
| NM_000784.3:c.1476+73G>A | NP_000775.1:n.1476+73G>A | |
| XM_017003488.2:c.1056+73G>A | XP_016858977.1:n.1056+73G>A | |
| NM_000784.4:c.1476+73G>A MANE Select | NP_000775.1:n.1476+73G>A |