Canonical Allele Identifier: CA988922391
Gene: DSG2 HGNC NCBI

Linked Data

dbSNP Id: rs2072992658
gnomAD v3: 18-31498166-C-T
gnomAD v4: 18-31498166-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498166C>T , CM000680.2:g.31498166C>T GRCh38
NC_000018.9:g.29078129C>T , CM000680.1:g.29078129C>T GRCh37
NC_000018.8:g.27332127C>T NCBI36
NG_007072.3:g.4925C>T , LRG_397:g.4925C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.12:c.-86C>T ENSP00000261590.8:n.-86C>T
NM_001943.3:c.-86C>T , LRG_397t1:c.-86C>T NP_001934.2:n.-86C>T
NM_001943.4:c.-86C>T NP_001934.2:n.-86C>T
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