HGVS | Genome Assembly |
---|---|
NC_000010.11:g.35638365T>C , CM000672.2:g.35638365T>C | GRCh38 |
NC_000010.10:g.35927293T>C , CM000672.1:g.35927293T>C | GRCh37 |
NC_000010.9:g.35967299T>C | NCBI36 |
NG_029968.1:g.8070A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374694.3:c.*980A>G MANE Select | ENSP00000363826.1:n.*980A>G | |
ENST00000374694.2:c.*980A>G | ENSP00000363826.1:n.*980A>G | |
NM_031866.2:c.*980A>G | NP_114072.1:n.*980A>G | |
NM_031866.3:c.*980A>G MANE Select | NP_114072.1:n.*980A>G |