Canonical Allele Identifier: CA644669568
Gene: MAGEC3 HGNC NCBI

Linked Data

dbSNP Id: rs1361878878
gnomAD v2: X-140982871-A-G
gnomAD v3: X-141895085-A-G
gnomAD v4: X-141895085-A-G
MyVariant Identifiers: chrX:g.140982871A>G (hg19) chrX:g.141895085A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895085A>G , CM000685.2:g.141895085A>G GRCh38
NC_000023.10:g.140982871A>G , CM000685.1:g.140982871A>G GRCh37
NC_000023.9:g.140810537A>G NCBI36
NG_013272.1:g.61770A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.910-184A>G MANE Select ENSP00000298296.1:n.910-184A>G
ENST00000443323.2:c.-118-1346A>G ENSP00000438254.1:n.-118-1346A>G
ENST00000483584.5:n.150-184A>G
ENST00000544766.5:c.-378-184A>G ENSP00000440444.1:n.-378-184A>G
NM_138702.1:c.910-184A>G MANE Select NP_619647.1:n.910-184A>G
NM_177456.2:c.-378-184A>G NP_803251.1:n.-378-184A>G
XM_017029265.2:c.-378-184A>G XP_016884754.1:n.-378-184A>G
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