Canonical Allele Identifier: CA402139296
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 924317
ClinVar RCV Id: RCV001185604 RCV004008541
dbSNP Id: rs2073196524
gnomAD v4: 18-31531192-G-A
MyVariant Identifiers: chr18:g.29111155G>A (hg19) chr18:g.31531192G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531192G>A , CM000680.2:g.31531192G>A GRCh38
NC_000018.9:g.29111155G>A , CM000680.1:g.29111155G>A GRCh37
NC_000018.8:g.27365153G>A NCBI36
NG_007072.3:g.37951G>A , LRG_397:g.37951G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000683614.2:n.1051G>A
ENST00000683614.1:c.1051G>A
ENST00000261590.13:c.1220G>A MANE Select ENSP00000261590.8:p.Gly407Asp
ENST00000261590.12:c.1220G>A ENSP00000261590.8:p.Gly407Asp
NM_001943.3:c.1220G>A , LRG_397t1:c.1220G>A NP_001934.2:p.Gly407Asp
NM_001943.4:c.1220G>A NP_001934.2:p.Gly407Asp
XM_024451095.1:c.686G>A XP_024306863.1:p.Gly229Asp
NM_001943.5:c.1220G>A MANE Select NP_001934.2:p.Gly407Asp
Search 100 bp 5'
Search 100 bp 3'