Canonical Allele Identifier: CA10532718
Gene: MAGEC3 HGNC NCBI

Linked Data

dbSNP Id: rs176026

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895341G>A , CM000685.2:g.141895341G>A GRCh38
NC_000023.10:g.140983127G>A , CM000685.1:g.140983127G>A GRCh37
NC_000023.9:g.140810793G>A NCBI36
NG_013272.1:g.62026G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000298296.1:n.982G>A MANE Select ENSP00000298296.1:p.Ala328Thr
ENST00000443323.2:c.-118-1090G>A ENSP00000438254.1:p.=
ENST00000483584.5:n.222G>A
ENST00000544766.5:c.-306G>A ENSP00000440444.1:p.=
NM_138702.1:n.982G>A MANE Select NP_619647.1:p.Ala328Thr
NM_177456.2:c.-306G>A NP_803251.1:p.=
XM_011531267.1:c.-229G>A XP_011529569.1:p.=
XM_011531267.3:c.-229G>A XP_011529569.1:p.=
XM_017029265.2:c.-306G>A XP_016884754.1:p.=