Canonical Allele Identifier: CA336129008
Gene: MAGEC3 HGNC NCBI

Linked Data

dbSNP Id: rs902107004
gnomAD v4: X-141895210-G-A
MyVariant Identifiers: chrX:g.140982996G>A (hg19) chrX:g.141895210G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895210G>A , CM000685.2:g.141895210G>A GRCh38
NC_000023.10:g.140982996G>A , CM000685.1:g.140982996G>A GRCh37
NC_000023.9:g.140810662G>A NCBI36
NG_013272.1:g.61895G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.910-59G>A MANE Select ENSP00000298296.1:n.910-59G>A
ENST00000443323.2:c.-118-1221G>A ENSP00000438254.1:n.-118-1221G>A
ENST00000483584.5:n.150-59G>A
ENST00000544766.5:c.-378-59G>A ENSP00000440444.1:n.-378-59G>A
NM_138702.1:c.910-59G>A MANE Select NP_619647.1:n.910-59G>A
NM_177456.2:c.-378-59G>A NP_803251.1:n.-378-59G>A
XM_011531267.1:c.-360G>A XP_011529569.1:n.-360G>A
XM_011531267.3:c.-360G>A XP_011529569.1:n.-360G>A
XM_017029265.2:c.-378-59G>A XP_016884754.1:n.-378-59G>A
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