Canonical Allele Identifier: CA391323462
Gene: MAGEL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.23889515G>T (hg19) chr15:g.23644368G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.23644368G>T , CM000677.2:g.23644368G>T GRCh38
NC_000015.9:g.23889515G>T , CM000677.1:g.23889515G>T GRCh37
NC_000015.8:g.21440608G>T NCBI36
NG_016776.1:g.8479C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650528.1:c.3375C>A MANE Select ENSP00000497810.1:p.Asn1125Lys
ENST00000532292.2:c.3375C>A ENSP00000433433.2:p.Asn1125Lys
NM_019066.4:c.3375C>A NP_061939.3:p.Asn1125Lys
NM_019066.5:c.3375C>A MANE Select NP_061939.3:p.Asn1125Lys
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