Canonical Allele Identifier: CA336129306

Gene: MAGEC3

Linked Data

• dbSNP Id: rs1032285297
• gnomAD v3: X-141895638-G-C
• gnomAD v4: X-141895638-G-C
• MyVariant Identifiers: chrX:g.140983424G>C (hg19) ; chrX:g.141895638G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.141895638G>C , CM000685.2:g.141895638G>C	GRCh38
NC_000023.10:g.140983424G>C , CM000685.1:g.140983424G>C	GRCh37
NC_000023.9:g.140811090G>C	NCBI36
NG_013272.1:g.62323G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298296.1:c.1123+79G>C MANE Select	ENSP00000298296.1:n.1123+79G>C
ENST00000443323.2:c.-118-793G>C	ENSP00000438254.1:n.-118-793G>C
ENST00000483584.5:n.288+231G>C
ENST00000544766.5:c.-240+231G>C	ENSP00000440444.1:n.-240+231G>C
NM_138702.1:c.1123+79G>C MANE Select	NP_619647.1:n.1123+79G>C
NM_177456.2:c.-240+231G>C	NP_803251.1:n.-240+231G>C
XM_011531267.1:c.-163+231G>C	XP_011529569.1:n.-163+231G>C
XM_011531267.3:c.-163+231G>C	XP_011529569.1:n.-163+231G>C
XM_017029265.2:c.-240+231G>C	XP_016884754.1:n.-240+231G>C