Canonical Allele Identifier: CA503600678
Gene: DSG2 HGNC NCBI

Linked Data

gnomAD v4: 18-31536233-C-A
MyVariant Identifiers: chr18:g.29116196C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31536233C>A , CM000680.2:g.31536233C>A GRCh38
NC_000018.9:g.29116196C>A , CM000680.1:g.29116196C>A GRCh37
NC_000018.8:g.27370194C>A NCBI36
NG_007072.3:g.42992C>A , LRG_397:g.42992C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1455C>A MANE Select ENSP00000261590.8:p.Val485=
ENST00000261590.12:c.1455C>A ENSP00000261590.8:p.Val485=
NM_001943.3:c.1455C>A , LRG_397t1:c.1455C>A NP_001934.2:p.Val485=
NM_001943.4:c.1455C>A NP_001934.2:p.Val485=
XM_024451095.1:c.921C>A XP_024306863.1:p.Val307=
NM_001943.5:c.1455C>A MANE Select NP_001934.2:p.Val485=
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