Canonical Allele Identifier: CA353434
Gene: MAGEL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 224132
ClinVar RCV Id: RCV000209903
dbSNP Id: rs869312694

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.23644535C>A , CM000677.2:g.23644535C>A GRCh38
NC_000015.9:g.23889682C>A , CM000677.1:g.23889682C>A GRCh37
NC_000015.8:g.21440775C>A NCBI36
NG_016776.1:g.8312G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650528.1:c.3208G>T MANE Select ENSP00000497810.1:p.Glu1070Ter
ENST00000532292.2:c.3208G>T ENSP00000433433.2:p.Glu1070Ter
NM_019066.4:c.3208G>T NP_061939.3:p.Glu1070Ter
NM_019066.5:c.3208G>T MANE Select NP_061939.3:p.Glu1070Ter