HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190388251G>T , CM000665.2:g.190388251G>T | GRCh38 |
NC_000003.11:g.190106040G>T , CM000665.1:g.190106040G>T | GRCh37 |
NC_000003.10:g.191588734G>T | NCBI36 |
NG_008149.1:g.5200G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264734.3:c.-79G>T MANE Select | ENSP00000264734.3:n.-79G>T | |
ENST00000456423.2:c.-79G>T | ENSP00000414136.2:n.-79G>T | |
ENST00000264734.2:c.132G>T | ENSP00000264734.2:p.Gln44His | |
ENST00000456423.1:c.132G>T | ENSP00000414136.1:p.Gln44His | |
ENST00000468220.1:n.306+13648G>T | ||
NM_006580.3:c.132G>T | NP_006571.1:p.Gln44His | |
NM_001378492.1:c.-79G>T | NP_001365421.1:n.-79G>T | |
NM_001378493.1:c.-79G>T | NP_001365422.1:n.-79G>T | |
NM_006580.4:c.-79G>T MANE Select | NP_006571.2:n.-79G>T |