Canonical Allele Identifier: CA2293845565
Gene: DSG2 HGNC NCBI

Linked Data

dbSNP Id: rs2072991859
gnomAD v4: 18-31498104-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498104A>C , CM000680.2:g.31498104A>C GRCh38
NC_000018.9:g.29078067A>C , CM000680.1:g.29078067A>C GRCh37
NC_000018.8:g.27332065A>C NCBI36
NG_007072.3:g.4863A>C , LRG_397:g.4863A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.12:c.-148A>C ENSP00000261590.8:n.-148A>C
NM_001943.3:c.-148A>C , LRG_397t1:c.-148A>C NP_001934.2:n.-148A>C
NM_001943.4:c.-148A>C NP_001934.2:n.-148A>C
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