Canonical Allele Identifier: CA503767178
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 753843
ClinVar RCV Id: RCV001494367 RCV001525135 RCV004003235
dbSNP Id: rs1195224927
gnomAD v3: 18-31546695-T-C
gnomAD v4: 18-31546695-T-C
MyVariant Identifiers: chr18:g.29126658T>C (hg19) chr18:g.31546695T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546695T>C , CM000680.2:g.31546695T>C GRCh38
NC_000018.9:g.29126658T>C , CM000680.1:g.29126658T>C GRCh37
NC_000018.8:g.27380656T>C NCBI36
NG_007072.3:g.53454T>C , LRG_397:g.53454T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3309T>C (DSG2) MANE Select ENSP00000261590.8:p.Ser1103=
ENST00000261590.12:c.3309T>C (DSG2) ENSP00000261590.8:p.Ser1103=
NM_001943.3:c.3309T>C , LRG_397t1:c.3309T>C (DSG2) NP_001934.2:p.Ser1103=
NR_045216.1:n.1346-789A>G (DSG2-AS1)
NM_001943.4:c.3309T>C (DSG2) NP_001934.2:p.Ser1103=
XM_024451095.1:c.2775T>C (DSG2) XP_024306863.1:p.Ser925=
NM_001943.5:c.3309T>C (DSG2) MANE Select NP_001934.2:p.Ser1103=
Search 100 bp 5'
Search 100 bp 3'