HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133532178C>A , CM000672.2:g.133532178C>A | GRCh38 |
NC_000010.10:g.135345682C>A , CM000672.1:g.135345682C>A | GRCh37 |
NC_000010.9:g.135195672C>A | NCBI36 |
NG_008383.1:g.9816C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000252945.8:c.542C>A MANE Select | ENSP00000252945.3:p.Ala181Asp | |
ENST00000252945.7:c.542C>A | ENSP00000252945.3:p.Ala181Asp | |
ENST00000368520.1:n.603C>A | ||
ENST00000418356.1:c.131C>A | ENSP00000397299.1:p.Ala44Asp | |
ENST00000421586.5:c.281C>A | ENSP00000412754.1:p.Ala94Asp | |
ENST00000463117.6:c.542C>A | ENSP00000440689.1:p.Ala181Asp | |
ENST00000477500.5:n.448+444C>A | ||
ENST00000541080.5:c.226+444C>A | ||
NM_000773.3:c.542C>A | NP_000764.1:p.Ala181Asp | |
NM_000773.4:c.542C>A MANE Select | NP_000764.1:p.Ala181Asp |