HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7525119T>C , CM000681.2:g.7525119T>C | GRCh38 |
NC_000019.9:g.7590005T>C , CM000681.1:g.7590005T>C | GRCh37 |
NC_000019.8:g.7496005T>C | NCBI36 |
NG_015806.1:g.7510T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.190T>C MANE Select | ENSP00000264079.5:p.Cys64Arg | |
ENST00000264079.10:c.190T>C | ENSP00000264079.5:p.Cys64Arg | |
ENST00000394321.9:n.270T>C | ||
ENST00000596390.1:n.306T>C | ||
ENST00000601003.1:c.190T>C | ENSP00000469074.1:p.Cys64Arg | |
NM_020533.2:c.190T>C | NP_065394.1:p.Cys64Arg | |
NM_020533.3:c.190T>C MANE Select | NP_065394.1:p.Cys64Arg |