HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133353855G>C , CM000671.2:g.133353855G>C | GRCh38 |
NC_000009.10:g.135210531G>C | NCBI36 |
NG_008477.1:g.7652C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371974.8:c.409C>G MANE Select | ENSP00000361042.3:p.Arg137Gly | |
ENST00000371974.7:c.409C>G | ENSP00000361042.3:p.Arg137Gly | |
ENST00000437995.1:n.355C>G | ||
ENST00000495952.5:n.399C>G | ||
ENST00000615505.4:c.82C>G | ENSP00000482067.1:p.Arg28Gly | |
NM_001280787.1:c.82C>G | NP_001267716.1:p.Arg28Gly | |
NM_003172.3:c.409C>G | NP_003163.1:p.Arg137Gly | |
XM_011518942.1:c.82C>G | XP_011517244.1:p.Arg28Gly | |
NM_003172.4:c.409C>G MANE Select | NP_003163.1:p.Arg137Gly |