HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20242661A>G , CM000684.2:g.20242661A>G | GRCh38 |
NC_000022.10:g.20230184A>G , CM000684.1:g.20230184A>G | GRCh37 |
NC_000022.9:g.18610184A>G | NCBI36 |
NG_012176.1:g.30633T>C | |
NG_012176.2:g.30633T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000043402.8:c.472T>C MANE Select | ENSP00000043402.7:p.Tyr158His | |
ENST00000043402.7:c.472T>C | ENSP00000043402.7:p.Tyr158His | |
ENST00000416372.5:c.531T>C | ||
ENST00000425986.1:c.729T>C | ||
ENST00000469601.1:n.608T>C | ||
NM_023004.5:c.472T>C | NP_075380.1:p.Tyr158His | |
NM_023004.6:c.472T>C MANE Select | NP_075380.1:p.Tyr158His |