Canonical Allele Identifier: CA413686514
Gene: MAGEE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.75004531C>A (hg19) chrX:g.75784696C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.75784696C>A , CM000685.2:g.75784696C>A GRCh38
NC_000023.10:g.75004531C>A , CM000685.1:g.75004531C>A GRCh37
NC_000023.9:g.74921256C>A NCBI36
NG_021324.1:g.5549G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373359.4:c.356G>T MANE Select ENSP00000362457.2:p.Arg119Ile
ENST00000373359.3:c.356G>T ENSP00000362457.2:p.Arg119Ile
NM_138703.4:c.356G>T NP_619648.1:p.Arg119Ile
XR_001755892.1:n.449-6596C>A
XR_001755894.1:n.449-6986C>A
NM_138703.5:c.356G>T MANE Select NP_619648.1:p.Arg119Ile
Search 100 bp 5'
Search 100 bp 3'