Canonical Allele Identifier: CA402148423
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1417616
ClinVar RCV Id: RCV001951831
dbSNP Id: rs2144361362
gnomAD v4: 18-31546486-G-T
MyVariant Identifiers: chr18:g.29126449G>T (hg19) chr18:g.31546486G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546486G>T , CM000680.2:g.31546486G>T GRCh38
NC_000018.9:g.29126449G>T , CM000680.1:g.29126449G>T GRCh37
NC_000018.8:g.27380447G>T NCBI36
NG_007072.3:g.53245G>T , LRG_397:g.53245G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.3100G>T (DSG2) MANE Select ENSP00000261590.8:p.Ala1034Ser
ENST00000261590.12:c.3100G>T (DSG2) ENSP00000261590.8:p.Ala1034Ser
NM_001943.3:c.3100G>T , LRG_397t1:c.3100G>T (DSG2) NP_001934.2:p.Ala1034Ser
NR_045216.1:n.1346-580C>A (DSG2-AS1)
NM_001943.4:c.3100G>T (DSG2) NP_001934.2:p.Ala1034Ser
XM_024451095.1:c.2566G>T (DSG2) XP_024306863.1:p.Ala856Ser
NM_001943.5:c.3100G>T (DSG2) MANE Select NP_001934.2:p.Ala1034Ser
Search 100 bp 5'
Search 100 bp 3'