Canonical Allele Identifier: CA413686511
Gene: MAGEE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.75004529C>T (hg19) chrX:g.75784694C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.75784694C>T , CM000685.2:g.75784694C>T GRCh38
NC_000023.10:g.75004529C>T , CM000685.1:g.75004529C>T GRCh37
NC_000023.9:g.74921254C>T NCBI36
NG_021324.1:g.5551G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373359.4:c.358G>A MANE Select ENSP00000362457.2:p.Glu120Lys
ENST00000373359.3:c.358G>A ENSP00000362457.2:p.Glu120Lys
NM_138703.4:c.358G>A NP_619648.1:p.Glu120Lys
XR_001755892.1:n.449-6598C>T
XR_001755894.1:n.449-6988C>T
NM_138703.5:c.358G>A MANE Select NP_619648.1:p.Glu120Lys
Search 100 bp 5'
Search 100 bp 3'