Canonical Allele Identifier: CA413686537
Gene: MAGEE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.75004541C>A (hg19) chrX:g.75784706C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.75784706C>A , CM000685.2:g.75784706C>A GRCh38
NC_000023.10:g.75004541C>A , CM000685.1:g.75004541C>A GRCh37
NC_000023.9:g.74921266C>A NCBI36
NG_021324.1:g.5539G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373359.4:c.346G>T MANE Select ENSP00000362457.2:p.Glu116Ter
ENST00000373359.3:c.346G>T ENSP00000362457.2:p.Glu116Ter
NM_138703.4:c.346G>T NP_619648.1:p.Glu116Ter
XR_001755892.1:n.449-6586C>A
XR_001755894.1:n.449-6976C>A
NM_138703.5:c.346G>T MANE Select NP_619648.1:p.Glu116Ter
Search 100 bp 5'
Search 100 bp 3'