Canonical Allele Identifier: CA413686519
Gene: MAGEE2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.75004534A>G (hg19) chrX:g.75784699A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.75784699A>G , CM000685.2:g.75784699A>G GRCh38
NC_000023.10:g.75004534A>G , CM000685.1:g.75004534A>G GRCh37
NC_000023.9:g.74921259A>G NCBI36
NG_021324.1:g.5546T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373359.4:c.353T>C MANE Select ENSP00000362457.2:p.Leu118Pro
ENST00000373359.3:c.353T>C ENSP00000362457.2:p.Leu118Pro
NM_138703.4:c.353T>C NP_619648.1:p.Leu118Pro
XR_001755892.1:n.449-6593A>G
XR_001755894.1:n.449-6983A>G
NM_138703.5:c.353T>C MANE Select NP_619648.1:p.Leu118Pro
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