HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154188T>G , CM000681.2:g.55154188T>G | GRCh38 |
NC_000019.9:g.55665556T>G , CM000681.1:g.55665556T>G | GRCh37 |
NC_000019.8:g.60357368T>G | NCBI36 |
NG_007866.2:g.8545A>C , LRG_432:g.8545A>C | |
NG_011829.2:g.51A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.391A>C MANE Select | ENSP00000341838.5:p.Lys131Gln | |
ENST00000665070.1:c.424A>C | ENSP00000499482.1:p.Lys142Gln | |
ENST00000344887.9:c.391A>C | ENSP00000341838.5:p.Lys131Gln | |
ENST00000585806.5:n.390A>C | ||
ENST00000586669.5:n.399A>C | ||
ENST00000588882.1:c.316A>C | ENSP00000466729.1:p.Lys106Gln | |
ENST00000589864.1:n.219A>C | ||
NM_000363.4:c.391A>C , LRG_432t1:c.391A>C | NP_000354.4:p.Lys131Gln | |
NM_000363.5:c.391A>C MANE Select | NP_000354.4:p.Lys131Gln |