Canonical Allele Identifier: CA414436419
Gene: MAGEC3 HGNC NCBI

Linked Data

dbSNP Id: rs2018080470
gnomAD v4: X-141895349-C-G
MyVariant Identifiers: chrX:g.140983135C>G (hg19) chrX:g.141895349C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895349C>G , CM000685.2:g.141895349C>G GRCh38
NC_000023.10:g.140983135C>G , CM000685.1:g.140983135C>G GRCh37
NC_000023.9:g.140810801C>G NCBI36
NG_013272.1:g.62034C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.990C>G MANE Select ENSP00000298296.1:p.Cys330Trp
ENST00000443323.2:c.-118-1082C>G ENSP00000438254.1:n.-118-1082C>G
ENST00000483584.5:n.230C>G
ENST00000544766.5:c.-298C>G ENSP00000440444.1:n.-298C>G
NM_138702.1:c.990C>G MANE Select NP_619647.1:p.Cys330Trp
NM_177456.2:c.-298C>G NP_803251.1:n.-298C>G
XM_011531267.1:c.-221C>G XP_011529569.1:n.-221C>G
XM_011531267.3:c.-221C>G XP_011529569.1:n.-221C>G
XM_017029265.2:c.-298C>G XP_016884754.1:n.-298C>G
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