Canonical Allele Identifier: CA402146731
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2073307298
gnomAD v4: 18-31546170-G-A
MyVariant Identifiers: chr18:g.29126133G>A (hg19) chr18:g.31546170G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546170G>A , CM000680.2:g.31546170G>A GRCh38
NC_000018.9:g.29126133G>A , CM000680.1:g.29126133G>A GRCh37
NC_000018.8:g.27380131G>A NCBI36
NG_007072.3:g.52929G>A , LRG_397:g.52929G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2784G>A (DSG2) MANE Select ENSP00000261590.8:p.Met928Ile
ENST00000261590.12:c.2784G>A (DSG2) ENSP00000261590.8:p.Met928Ile
NM_001943.3:c.2784G>A , LRG_397t1:c.2784G>A (DSG2) NP_001934.2:p.Met928Ile
NR_045216.1:n.1346-264C>T (DSG2-AS1)
NM_001943.4:c.2784G>A (DSG2) NP_001934.2:p.Met928Ile
XM_024451095.1:c.2250G>A (DSG2) XP_024306863.1:p.Met750Ile
NM_001943.5:c.2784G>A (DSG2) MANE Select NP_001934.2:p.Met928Ile
Search 100 bp 5'
Search 100 bp 3'