Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.72198345C>T , CM000667.2:g.72198345C>T | GRCh38 |
| NC_000005.9:g.71494172C>T , CM000667.1:g.71494172C>T | GRCh37 |
| NC_000005.8:g.71529928C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005909.5:c.4990C>T MANE Select | NP_005900.2:p.Arg1664Ter |
| ENST00000296755.12:c.4990C>T MANE Select | ENSP00000296755.7:p.Arg1664Ter |
| NM_001324255.1:c.4612C>T | NP_001311184.1:p.Arg1538Ter |
| NM_001324255.2:c.4612C>T | NP_001311184.1:p.Arg1538Ter |
| NM_005909.3:c.4990C>T | NP_005900.2:p.Arg1664Ter |
| NM_005909.4:c.4990C>T | NP_005900.2:p.Arg1664Ter |
| ENST00000296755.11:c.4990C>T | ENSP00000296755.7:p.Arg1664Ter |
| XM_005248507.2:c.4612C>T | XP_005248564.1:p.Arg1538Ter |