Canonical Allele Identifier: CA2293859908
Gene: DSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1598816654
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531418G>A , CM000680.2:g.31531418G>A GRCh38
NC_000018.9:g.29111381G>A , CM000680.1:g.29111381G>A GRCh37
NC_000018.8:g.27365379G>A NCBI36
NG_007072.3:g.38177G>A , LRG_397:g.38177G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000683614.2:n.1277G>A
ENST00000683614.1:c.1277G>A
ENST00000261590.13:c.1280+166G>A MANE Select ENSP00000261590.8:n.1280+166G>A
ENST00000261590.12:c.1280+166G>A ENSP00000261590.8:n.1280+166G>A
NM_001943.3:c.1280+166G>A , LRG_397t1:c.1280+166G>A NP_001934.2:n.1280+166G>A
NM_001943.4:c.1280+166G>A NP_001934.2:n.1280+166G>A
XM_024451095.1:c.746+166G>A XP_024306863.1:n.746+166G>A
NM_001943.5:c.1280+166G>A MANE Select NP_001934.2:n.1280+166G>A
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