Canonical Allele Identifier: CA297703028

Gene: DSG2 DSG2-AS1

Linked Data

• dbSNP Id: rs11542764
• MyVariant Identifiers: chr18:g.29127188A>G (hg19) ; chr18:g.31547225A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31547225A>G , CM000680.2:g.31547225A>G	GRCh38
NC_000018.9:g.29127188A>G , CM000680.1:g.29127188A>G	GRCh37
NC_000018.8:g.27381186A>G	NCBI36
NG_007072.3:g.53984A>G , LRG_397:g.53984A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261590.13:c.*482A>G (DSG2) MANE Select	ENSP00000261590.8:n.*482A>G
ENST00000261590.12:c.*482A>G (DSG2)	ENSP00000261590.8:n.*482A>G
NM_001943.3:c.*482A>G , LRG_397t1:c.*482A>G (DSG2)	NP_001934.2:n.*482A>G
NR_045216.1:n.1346-1319T>C (DSG2-AS1)
NM_001943.4:c.*482A>G (DSG2)	NP_001934.2:n.*482A>G
XM_024451095.1:c.*482A>G (DSG2)	XP_024306863.1:n.*482A>G
NM_001943.5:c.*482A>G (DSG2) MANE Select	NP_001934.2:n.*482A>G