Canonical Allele Identifier: CA778427329
Gene: DSG2 HGNC NCBI

Linked Data

dbSNP Id: rs149048465
gnomAD v3: 18-31498158-G-A
gnomAD v4: 18-31498158-G-A
MyVariant Identifiers: chr18:g.29078121G>A (hg19) chr18:g.31498158G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498158G>A , CM000680.2:g.31498158G>A GRCh38
NC_000018.9:g.29078121G>A , CM000680.1:g.29078121G>A GRCh37
NC_000018.8:g.27332119G>A NCBI36
NG_007072.3:g.4917G>A , LRG_397:g.4917G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.12:c.-94G>A ENSP00000261590.8:n.-94G>A
NM_001943.3:c.-94G>A , LRG_397t1:c.-94G>A NP_001934.2:n.-94G>A
NM_001943.4:c.-94G>A NP_001934.2:n.-94G>A
Search 100 bp 5'
Search 100 bp 3'