Canonical Allele Identifier: CA517468903
Gene: MAGEE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.75004533G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.75784698G>T , CM000685.2:g.75784698G>T GRCh38
NC_000023.10:g.75004533G>T , CM000685.1:g.75004533G>T GRCh37
NC_000023.9:g.74921258G>T NCBI36
NG_021324.1:g.5547C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373359.4:c.354C>A MANE Select ENSP00000362457.2:p.Leu118=
ENST00000373359.3:c.354C>A ENSP00000362457.2:p.Leu118=
NM_138703.4:c.354C>A NP_619648.1:p.Leu118=
XR_001755892.1:n.449-6594G>T
XR_001755894.1:n.449-6984G>T
NM_138703.5:c.354C>A MANE Select NP_619648.1:p.Leu118=
Search 100 bp 5'
Search 100 bp 3'