Canonical Allele Identifier: CA2641405592
Gene: DSG2 HGNC NCBI

Linked Data

gnomAD v4: 18-31498173-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498173C>A , CM000680.2:g.31498173C>A GRCh38
NC_000018.9:g.29078136C>A , CM000680.1:g.29078136C>A GRCh37
NC_000018.8:g.27332134C>A NCBI36
NG_007072.3:g.4932C>A , LRG_397:g.4932C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.12:c.-79C>A ENSP00000261590.8:n.-79C>A
NM_001943.3:c.-79C>A , LRG_397t1:c.-79C>A NP_001934.2:n.-79C>A
NM_001943.4:c.-79C>A NP_001934.2:n.-79C>A
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