HGVS | Genome Assembly |
---|---|
NC_000008.11:g.6877881G>T , CM000670.2:g.6877881G>T | GRCh38 |
NC_000008.10:g.6735403G>T , CM000670.1:g.6735403G>T | GRCh37 |
NC_000008.9:g.6722813G>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297439.4:c.-24C>A MANE Select | ENSP00000297439.3:n.-24C>A | |
ENST00000297439.3:c.-24C>A | ENSP00000297439.3:n.-24C>A | |
NM_005218.3:c.-24C>A | NP_005209.1:n.-24C>A | |
NM_005218.4:c.-24C>A MANE Select | NP_005209.1:n.-24C>A |