Canonical Allele Identifier: CA1137911157
Gene: MAGEC3 HGNC NCBI

Linked Data

dbSNP Id: rs2018076400
gnomAD v3: X-141895110-G-C
gnomAD v4: X-141895110-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895110G>C , CM000685.2:g.141895110G>C GRCh38
NC_000023.10:g.140982896G>C , CM000685.1:g.140982896G>C GRCh37
NC_000023.9:g.140810562G>C NCBI36
NG_013272.1:g.61795G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.910-159G>C MANE Select ENSP00000298296.1:n.910-159G>C
ENST00000443323.2:c.-118-1321G>C ENSP00000438254.1:n.-118-1321G>C
ENST00000483584.5:n.150-159G>C
ENST00000544766.5:c.-378-159G>C ENSP00000440444.1:n.-378-159G>C
NM_138702.1:c.910-159G>C MANE Select NP_619647.1:n.910-159G>C
NM_177456.2:c.-378-159G>C NP_803251.1:n.-378-159G>C
XM_017029265.2:c.-378-159G>C XP_016884754.1:n.-378-159G>C
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