Canonical Allele Identifier: CA402141780
Gene: DSG2 HGNC NCBI

Linked Data

dbSNP Id: rs778119035
gnomAD v3: 18-31536333-G-A
gnomAD v4: 18-31536333-G-A
MyVariant Identifiers: chr18:g.29116296G>A (hg19) chr18:g.31536333G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31536333G>A , CM000680.2:g.31536333G>A GRCh38
NC_000018.9:g.29116296G>A , CM000680.1:g.29116296G>A GRCh37
NC_000018.8:g.27370294G>A NCBI36
NG_007072.3:g.43092G>A , LRG_397:g.43092G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1555G>A MANE Select ENSP00000261590.8:p.Asp519Asn
ENST00000261590.12:c.1555G>A ENSP00000261590.8:p.Asp519Asn
NM_001943.3:c.1555G>A , LRG_397t1:c.1555G>A NP_001934.2:p.Asp519Asn
NM_001943.4:c.1555G>A NP_001934.2:p.Asp519Asn
XM_024451095.1:c.1021G>A XP_024306863.1:p.Asp341Asn
NM_001943.5:c.1555G>A MANE Select NP_001934.2:p.Asp519Asn
Search 100 bp 5'
Search 100 bp 3'