HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7454405A>C , CM000679.2:g.7454405A>C | GRCh38 |
NC_000017.10:g.7357724A>C , CM000679.1:g.7357724A>C | GRCh37 |
NC_000017.9:g.7298448A>C | NCBI36 |
NG_008026.1:g.14319A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000306071.7:c.929A>C MANE Select | ENSP00000304290.2:p.Lys310Thr | |
ENST00000306071.6:c.929A>C | ENSP00000304290.2:p.Lys310Thr | |
ENST00000536404.6:c.713A>C | ENSP00000439209.2:p.Lys238Thr | |
ENST00000570557.5:c.592A>C | ||
ENST00000573209.1:n.1873A>C | ||
ENST00000576360.1:c.605-39A>C | ENSP00000459092.1:n.605-39A>C | |
NM_000747.2:c.929A>C | NP_000738.2:p.Lys310Thr | |
NM_000747.3:c.929A>C MANE Select | NP_000738.2:p.Lys310Thr |