Canonical Allele Identifier: CA10532719
Gene: MAGEC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2570323
ClinVar RCV Id: RCV003289062
dbSNP Id: rs200912965
ExAC: X:140983151 A / G
gnomAD v2: X-140983151-A-G
gnomAD v3: X-141895365-A-G
gnomAD v4: X-141895365-A-G
MyVariant Identifiers: chrX:g.140983151A>G (hg19) chrX:g.141895365A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895365A>G , CM000685.2:g.141895365A>G GRCh38
NC_000023.10:g.140983151A>G , CM000685.1:g.140983151A>G GRCh37
NC_000023.9:g.140810817A>G NCBI36
NG_013272.1:g.62050A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298296.1:c.1006A>G MANE Select ENSP00000298296.1:p.Arg336Gly
ENST00000443323.2:c.-118-1066A>G ENSP00000438254.1:n.-118-1066A>G
ENST00000483584.5:n.246A>G
ENST00000544766.5:c.-282A>G ENSP00000440444.1:n.-282A>G
NM_138702.1:c.1006A>G MANE Select NP_619647.1:p.Arg336Gly
NM_177456.2:c.-282A>G NP_803251.1:n.-282A>G
XM_011531267.1:c.-205A>G XP_011529569.1:n.-205A>G
XM_011531267.3:c.-205A>G XP_011529569.1:n.-205A>G
XM_017029265.2:c.-282A>G XP_016884754.1:n.-282A>G
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