Canonical Allele Identifier: CA413686530
Gene: MAGEE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.75004538A>C (hg19) chrX:g.75784703A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.75784703A>C , CM000685.2:g.75784703A>C GRCh38
NC_000023.10:g.75004538A>C , CM000685.1:g.75004538A>C GRCh37
NC_000023.9:g.74921263A>C NCBI36
NG_021324.1:g.5542T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373359.4:c.349T>G MANE Select ENSP00000362457.2:p.Phe117Val
ENST00000373359.3:c.349T>G ENSP00000362457.2:p.Phe117Val
NM_138703.4:c.349T>G NP_619648.1:p.Phe117Val
XR_001755892.1:n.449-6589A>C
XR_001755894.1:n.449-6979A>C
NM_138703.5:c.349T>G MANE Select NP_619648.1:p.Phe117Val
Search 100 bp 5'
Search 100 bp 3'