Canonical Allele Identifier: CA297703252
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs970356448
gnomAD v3: 18-31547452-G-C
gnomAD v4: 18-31547452-G-C
MyVariant Identifiers: chr18:g.29127415G>C (hg19) chr18:g.31547452G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547452G>C , CM000680.2:g.31547452G>C GRCh38
NC_000018.9:g.29127415G>C , CM000680.1:g.29127415G>C GRCh37
NC_000018.8:g.27381413G>C NCBI36
NG_007072.3:g.54211G>C , LRG_397:g.54211G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*709G>C (DSG2) MANE Select ENSP00000261590.8:n.*709G>C
ENST00000261590.12:c.*709G>C (DSG2) ENSP00000261590.8:n.*709G>C
NM_001943.3:c.*709G>C , LRG_397t1:c.*709G>C (DSG2) NP_001934.2:n.*709G>C
NR_045216.1:n.1346-1546C>G (DSG2-AS1)
NM_001943.4:c.*709G>C (DSG2) NP_001934.2:n.*709G>C
XM_024451095.1:c.*709G>C (DSG2) XP_024306863.1:n.*709G>C
NM_001943.5:c.*709G>C (DSG2) MANE Select NP_001934.2:n.*709G>C
Search 100 bp 5'
Search 100 bp 3'