Canonical Allele Identifier: CA297700080
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 576360
ClinVar RCV Id: RCV000698840 RCV001187930
dbSNP Id: rs1036247495
gnomAD v4: 18-31542524-T-A
MyVariant Identifiers: chr18:g.29122487T>A (hg19) chr18:g.31542524T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542524T>A , CM000680.2:g.31542524T>A GRCh38
NC_000018.9:g.29122487T>A , CM000680.1:g.29122487T>A GRCh37
NC_000018.8:g.27376485T>A NCBI36
NG_007072.3:g.49283T>A , LRG_397:g.49283T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2006T>A (DSG2) MANE Select ENSP00000261590.8:p.Val669Glu
ENST00000261590.12:c.2006T>A (DSG2) ENSP00000261590.8:p.Val669Glu
NM_001943.3:c.2006T>A , LRG_397t1:c.2006T>A (DSG2) NP_001934.2:p.Val669Glu
NR_045216.1:n.1811-203A>T (DSG2-AS1)
NM_001943.4:c.2006T>A (DSG2) NP_001934.2:p.Val669Glu
XM_024451095.1:c.1472T>A (DSG2) XP_024306863.1:p.Val491Glu
NM_001943.5:c.2006T>A (DSG2) MANE Select NP_001934.2:p.Val669Glu
Search 100 bp 5'
Search 100 bp 3'