HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119651465C>A , CM000672.2:g.119651465C>A | GRCh38 |
NC_000010.10:g.121410977C>A , CM000672.1:g.121410977C>A | GRCh37 |
NC_000010.9:g.121400967C>A | NCBI36 |
NG_016125.1:g.5096C>A , LRG_742:g.5096C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.-211C>A MANE Select | ENSP00000358081.4:n.-211C>A | |
ENST00000369085.7:c.-211C>A | ENSP00000358081.3:n.-211C>A | |
NM_004281.3:c.-211C>A , LRG_742t1:c.-211C>A | NP_004272.2:n.-211C>A | |
XM_005270287.1:c.-211C>A | XP_005270344.1:n.-211C>A | |
XM_005270287.2:c.-211C>A | XP_005270344.1:n.-211C>A | |
NM_004281.4:c.-211C>A MANE Select | NP_004272.2:n.-211C>A |