Canonical Allele Identifier: CA297712985
Gene: DSG2 HGNC NCBI

Linked Data

dbSNP Id: rs932207042
gnomAD v3: 18-31498170-G-T
gnomAD v4: 18-31498170-G-T
MyVariant Identifiers: chr18:g.29078133G>T (hg19) chr18:g.31498170G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498170G>T , CM000680.2:g.31498170G>T GRCh38
NC_000018.9:g.29078133G>T , CM000680.1:g.29078133G>T GRCh37
NC_000018.8:g.27332131G>T NCBI36
NG_007072.3:g.4929G>T , LRG_397:g.4929G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.12:c.-82G>T ENSP00000261590.8:n.-82G>T
NM_001943.3:c.-82G>T , LRG_397t1:c.-82G>T NP_001934.2:n.-82G>T
NM_001943.4:c.-82G>T NP_001934.2:n.-82G>T
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