Canonical Allele Identifier: CA517468913
Gene: MAGEE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.75004542C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.75784707C>A , CM000685.2:g.75784707C>A GRCh38
NC_000023.10:g.75004542C>A , CM000685.1:g.75004542C>A GRCh37
NC_000023.9:g.74921267C>A NCBI36
NG_021324.1:g.5538G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373359.4:c.345G>T MANE Select ENSP00000362457.2:p.Leu115=
ENST00000373359.3:c.345G>T ENSP00000362457.2:p.Leu115=
NM_138703.4:c.345G>T NP_619648.1:p.Leu115=
XR_001755892.1:n.449-6585C>A
XR_001755894.1:n.449-6975C>A
NM_138703.5:c.345G>T MANE Select NP_619648.1:p.Leu115=
Search 100 bp 5'
Search 100 bp 3'