Canonical Allele Identifier: CA517468902
Gene: MAGEE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.75004532T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.75784697T>G , CM000685.2:g.75784697T>G GRCh38
NC_000023.10:g.75004532T>G , CM000685.1:g.75004532T>G GRCh37
NC_000023.9:g.74921257T>G NCBI36
NG_021324.1:g.5548A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373359.4:c.355A>C MANE Select ENSP00000362457.2:p.Arg119=
ENST00000373359.3:c.355A>C ENSP00000362457.2:p.Arg119=
NM_138703.4:c.355A>C NP_619648.1:p.Arg119=
XR_001755892.1:n.449-6595T>G
XR_001755894.1:n.449-6985T>G
NM_138703.5:c.355A>C MANE Select NP_619648.1:p.Arg119=
Search 100 bp 5'
Search 100 bp 3'