Canonical Allele Identifier: CA10641351
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 326464
ClinVar RCV Id: RCV000392535
dbSNP Id: rs886053709

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498117A>T , CM000680.2:g.31498117A>T GRCh38
NC_000018.9:g.29078080A>T , CM000680.1:g.29078080A>T GRCh37
NC_000018.8:g.27332078A>T NCBI36
NG_007072.3:g.4876A>T , LRG_397:g.4876A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.12:c.-135A>T ENSP00000261590.8:n.-135A>T
NM_001943.3:c.-135A>T , LRG_397t1:c.-135A>T NP_001934.2:n.-135A>T
NM_001943.4:c.-135A>T NP_001934.2:n.-135A>T