Canonical Allele Identifier: CA391324000
Gene: MAGEL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.23889617G>C (hg19) chr15:g.23644470G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.23644470G>C , CM000677.2:g.23644470G>C GRCh38
NC_000015.9:g.23889617G>C , CM000677.1:g.23889617G>C GRCh37
NC_000015.8:g.21440710G>C NCBI36
NG_016776.1:g.8377C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650528.1:c.3273C>G MANE Select ENSP00000497810.1:p.Asn1091Lys
ENST00000532292.2:c.3273C>G ENSP00000433433.2:p.Asn1091Lys
NM_019066.4:c.3273C>G NP_061939.3:p.Asn1091Lys
NM_019066.5:c.3273C>G MANE Select NP_061939.3:p.Asn1091Lys
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