Canonical Allele Identifier: CA778427334
Gene: DSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1014659603
gnomAD v3: 18-31498159-G-T
gnomAD v4: 18-31498159-G-T
MyVariant Identifiers: chr18:g.29078122G>T (hg19) chr18:g.31498159G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498159G>T , CM000680.2:g.31498159G>T GRCh38
NC_000018.9:g.29078122G>T , CM000680.1:g.29078122G>T GRCh37
NC_000018.8:g.27332120G>T NCBI36
NG_007072.3:g.4918G>T , LRG_397:g.4918G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.12:c.-93G>T ENSP00000261590.8:n.-93G>T
NM_001943.3:c.-93G>T , LRG_397t1:c.-93G>T NP_001934.2:n.-93G>T
NM_001943.4:c.-93G>T NP_001934.2:n.-93G>T
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