Canonical Allele Identifier: CA988913886
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2073316473

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546890A>G , CM000680.2:g.31546890A>G GRCh38
NC_000018.9:g.29126853A>G , CM000680.1:g.29126853A>G GRCh37
NC_000018.8:g.27380851A>G NCBI36
NG_007072.3:g.53649A>G , LRG_397:g.53649A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*147A>G (DSG2) MANE Select ENSP00000261590.8:n.*147A>G
ENST00000261590.12:c.*147A>G (DSG2) ENSP00000261590.8:n.*147A>G
NM_001943.3:c.*147A>G , LRG_397t1:c.*147A>G (DSG2) NP_001934.2:n.*147A>G
NR_045216.1:n.1346-984T>C (DSG2-AS1)
NM_001943.4:c.*147A>G (DSG2) NP_001934.2:n.*147A>G
XM_024451095.1:c.*147A>G (DSG2) XP_024306863.1:n.*147A>G
NM_001943.5:c.*147A>G (DSG2) MANE Select NP_001934.2:n.*147A>G