Canonical Allele Identifier: CA872279866
Gene: MAGEC3 HGNC NCBI

Linked Data

dbSNP Id: rs1255379342
MyVariant Identifiers: chrX:g.140983419T>C (hg19) chrX:g.141895633T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.141895633T>C , CM000685.2:g.141895633T>C GRCh38
NC_000023.10:g.140983419T>C , CM000685.1:g.140983419T>C GRCh37
NC_000023.9:g.140811085T>C NCBI36
NG_013272.1:g.62318T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298296.1:c.1123+74T>C MANE Select ENSP00000298296.1:n.1123+74T>C
ENST00000443323.2:c.-118-798T>C ENSP00000438254.1:n.-118-798T>C
ENST00000483584.5:n.288+226T>C
ENST00000544766.5:c.-240+226T>C ENSP00000440444.1:n.-240+226T>C
NM_138702.1:c.1123+74T>C MANE Select NP_619647.1:n.1123+74T>C
NM_177456.2:c.-240+226T>C NP_803251.1:n.-240+226T>C
XM_011531267.1:c.-163+226T>C XP_011529569.1:n.-163+226T>C
XM_011531267.3:c.-163+226T>C XP_011529569.1:n.-163+226T>C
XM_017029265.2:c.-240+226T>C XP_016884754.1:n.-240+226T>C
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