Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.31393651G>A , CM000676.2:g.31393651G>A | GRCh38 |
| NC_000014.8:g.31862857G>A , CM000676.1:g.31862857G>A | GRCh37 |
| NC_000014.7:g.30932608G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000543095.7:c.772+401C>T MANE Select | ENSP00000437968.2:n.772+401C>T | |
| ENST00000543095.6:c.772+401C>T | ENSP00000437968.2:n.772+401C>T | |
| ENST00000549185.5:c.*868+401C>T | ENSP00000446654.1:n.*868+401C>T | |
| NM_015473.3:c.772+401C>T | NP_056288.2:n.772+401C>T | |
| NM_015473.4:c.772+401C>T MANE Select | NP_056288.2:n.772+401C>T |