HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20242678C>T , CM000684.2:g.20242678C>T | GRCh38 |
NC_000022.10:g.20230201C>T , CM000684.1:g.20230201C>T | GRCh37 |
NC_000022.9:g.18610201C>T | NCBI36 |
NG_012176.1:g.30616G>A | |
NG_012176.2:g.30616G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000043402.8:c.455G>A MANE Select | ENSP00000043402.7:p.Gly152Asp | |
ENST00000043402.7:c.455G>A | ENSP00000043402.7:p.Gly152Asp | |
ENST00000416372.5:c.514G>A | ||
ENST00000425986.1:c.712G>A | ||
ENST00000469601.1:n.591G>A | ||
NM_023004.5:c.455G>A | NP_075380.1:p.Gly152Asp | |
NM_023004.6:c.455G>A MANE Select | NP_075380.1:p.Gly152Asp |