Canonical Allele Identifier: CA297703291
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs978263951
gnomAD v3: 18-31547538-G-A
gnomAD v4: 18-31547538-G-A
MyVariant Identifiers: chr18:g.29127501G>A (hg19) chr18:g.31547538G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547538G>A , CM000680.2:g.31547538G>A GRCh38
NC_000018.9:g.29127501G>A , CM000680.1:g.29127501G>A GRCh37
NC_000018.8:g.27381499G>A NCBI36
NG_007072.3:g.54297G>A , LRG_397:g.54297G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*795G>A (DSG2) MANE Select ENSP00000261590.8:n.*795G>A
ENST00000261590.12:c.*795G>A (DSG2) ENSP00000261590.8:n.*795G>A
NM_001943.3:c.*795G>A , LRG_397t1:c.*795G>A (DSG2) NP_001934.2:n.*795G>A
NR_045216.1:n.1346-1632C>T (DSG2-AS1)
NM_001943.4:c.*795G>A (DSG2) NP_001934.2:n.*795G>A
NM_001943.5:c.*795G>A (DSG2) MANE Select NP_001934.2:n.*795G>A
Search 100 bp 5'
Search 100 bp 3'