Canonical Allele Identifier: CA503766188
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1185207295
gnomAD v2: 18-29125986-G-A
MyVariant Identifiers: chr18:g.29125986G>A (hg19) chr18:g.31546023G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546023G>A , CM000680.2:g.31546023G>A GRCh38
NC_000018.9:g.29125986G>A , CM000680.1:g.29125986G>A GRCh37
NC_000018.8:g.27379984G>A NCBI36
NG_007072.3:g.52782G>A , LRG_397:g.52782G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2637G>A (DSG2) MANE Select ENSP00000261590.8:p.Glu879=
ENST00000261590.12:c.2637G>A (DSG2) ENSP00000261590.8:p.Glu879=
NM_001943.3:c.2637G>A , LRG_397t1:c.2637G>A (DSG2) NP_001934.2:p.Glu879=
NR_045216.1:n.1346-117C>T (DSG2-AS1)
NM_001943.4:c.2637G>A (DSG2) NP_001934.2:p.Glu879=
XM_024451095.1:c.2103G>A (DSG2) XP_024306863.1:p.Glu701=
NM_001943.5:c.2637G>A (DSG2) MANE Select NP_001934.2:p.Glu879=
Search 100 bp 5'
Search 100 bp 3'