Canonical Allele Identifier: CA629148140

Gene: DSG2

Linked Data

• dbSNP Id: rs1371732738
• gnomAD v2: 18-29104574-T-G
• gnomAD v4: 18-31524611-T-G
• MyVariant Identifiers: chr18:g.29104574T>G (hg19) ; chr18:g.31524611T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31524611T>G , CM000680.2:g.31524611T>G	GRCh38
NC_000018.9:g.29104574T>G , CM000680.1:g.29104574T>G	GRCh37
NC_000018.8:g.27358572T>G	NCBI36
NG_007072.3:g.31370T>G , LRG_397:g.31370T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682087.2:n.659+26T>G
ENST00000683614.2:n.659+26T>G
ENST00000682087.1:c.659+26T>G
ENST00000683614.1:c.659+26T>G
ENST00000261590.13:c.828+26T>G MANE Select	ENSP00000261590.8:n.828+26T>G
ENST00000261590.12:c.828+26T>G	ENSP00000261590.8:n.828+26T>G
NM_001943.3:c.828+26T>G , LRG_397t1:c.828+26T>G	NP_001934.2:n.828+26T>G
NM_001943.4:c.828+26T>G	NP_001934.2:n.828+26T>G
XM_024451095.1:c.294+26T>G	XP_024306863.1:n.294+26T>G
NM_001943.5:c.828+26T>G MANE Select	NP_001934.2:n.828+26T>G