Canonical Allele Identifier: CA517468899
Gene: MAGEE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.75004530T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.75784695T>C , CM000685.2:g.75784695T>C GRCh38
NC_000023.10:g.75004530T>C , CM000685.1:g.75004530T>C GRCh37
NC_000023.9:g.74921255T>C NCBI36
NG_021324.1:g.5550A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000373359.4:c.357A>G MANE Select ENSP00000362457.2:p.Arg119=
ENST00000373359.3:c.357A>G ENSP00000362457.2:p.Arg119=
NM_138703.4:c.357A>G NP_619648.1:p.Arg119=
XR_001755892.1:n.449-6597T>C
XR_001755894.1:n.449-6987T>C
NM_138703.5:c.357A>G MANE Select NP_619648.1:p.Arg119=
Search 100 bp 5'
Search 100 bp 3'