Canonical Allele Identifier: CA297703254
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs981701697
gnomAD v2: 18-29127421-A-G
gnomAD v3: 18-31547458-A-G
gnomAD v4: 18-31547458-A-G
COSMIC: COSN26779366
MyVariant Identifiers: chr18:g.29127421A>G (hg19) chr18:g.31547458A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547458A>G , CM000680.2:g.31547458A>G GRCh38
NC_000018.9:g.29127421A>G , CM000680.1:g.29127421A>G GRCh37
NC_000018.8:g.27381419A>G NCBI36
NG_007072.3:g.54217A>G , LRG_397:g.54217A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*715A>G (DSG2) MANE Select ENSP00000261590.8:n.*715A>G
ENST00000261590.12:c.*715A>G (DSG2) ENSP00000261590.8:n.*715A>G
NM_001943.3:c.*715A>G , LRG_397t1:c.*715A>G (DSG2) NP_001934.2:n.*715A>G
NR_045216.1:n.1346-1552T>C (DSG2-AS1)
NM_001943.4:c.*715A>G (DSG2) NP_001934.2:n.*715A>G
XM_024451095.1:c.*715A>G (DSG2) XP_024306863.1:n.*715A>G
NM_001943.5:c.*715A>G (DSG2) MANE Select NP_001934.2:n.*715A>G
Search 100 bp 5'
Search 100 bp 3'