Canonical Allele Identifier: CA10456607
Gene: MAGEE2 HGNC NCBI

Linked Data

dbSNP Id: rs1343879
gnomAD v2: X-75004529-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.75784694C>G , CM000685.2:g.75784694C>G GRCh38
NC_000023.10:g.75004529C>G , CM000685.1:g.75004529C>G GRCh37
NC_000023.9:g.74921254C>G NCBI36
NG_021324.1:g.5551G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000373359.4:c.358G>C MANE Select ENSP00000362457.2:p.Glu120Gln
ENST00000373359.3:c.358G>C ENSP00000362457.2:p.Glu120Gln
NM_138703.4:c.358G>C NP_619648.1:p.Glu120Gln
XR_001755892.1:n.449-6598C>G
XR_001755894.1:n.449-6988C>G
NM_138703.5:c.358G>C MANE Select NP_619648.1:p.Glu120Gln