Canonical Allele Identifier: CA336128986
Gene: MAGEC3 HGNC NCBI

Linked Data

dbSNP Id: rs868256344
gnomAD v2: X-140982907-T-G
gnomAD v3: X-141895121-T-G
gnomAD v4: X-141895121-T-G
MyVariant Identifiers: chrX:g.140982907T>G (hg19) chrX:g.141895121T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895121T>G , CM000685.2:g.141895121T>G GRCh38
NC_000023.10:g.140982907T>G , CM000685.1:g.140982907T>G GRCh37
NC_000023.9:g.140810573T>G NCBI36
NG_013272.1:g.61806T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.910-148T>G MANE Select ENSP00000298296.1:n.910-148T>G
ENST00000443323.2:c.-118-1310T>G ENSP00000438254.1:n.-118-1310T>G
ENST00000483584.5:n.150-148T>G
ENST00000544766.5:c.-378-148T>G ENSP00000440444.1:n.-378-148T>G
NM_138702.1:c.910-148T>G MANE Select NP_619647.1:n.910-148T>G
NM_177456.2:c.-378-148T>G NP_803251.1:n.-378-148T>G
XM_017029265.2:c.-378-148T>G XP_016884754.1:n.-378-148T>G
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