Canonical Allele Identifier: CA413686536
Gene: MAGEE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.75004540T>C (hg19) chrX:g.75784705T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.75784705T>C , CM000685.2:g.75784705T>C GRCh38
NC_000023.10:g.75004540T>C , CM000685.1:g.75004540T>C GRCh37
NC_000023.9:g.74921265T>C NCBI36
NG_021324.1:g.5540A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373359.4:c.347A>G MANE Select ENSP00000362457.2:p.Glu116Gly
ENST00000373359.3:c.347A>G ENSP00000362457.2:p.Glu116Gly
NM_138703.4:c.347A>G NP_619648.1:p.Glu116Gly
XR_001755892.1:n.449-6587T>C
XR_001755894.1:n.449-6977T>C
NM_138703.5:c.347A>G MANE Select NP_619648.1:p.Glu116Gly
Search 100 bp 5'
Search 100 bp 3'