Canonical Allele Identifier: CA047737
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs750956420

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546406A>G , CM000680.2:g.31546406A>G GRCh38
NC_000018.9:g.29126369A>G , CM000680.1:g.29126369A>G GRCh37
NC_000018.8:g.27380367A>G NCBI36
NG_007072.3:g.53165A>G , LRG_397:g.53165A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.3020A>G (DSG2) MANE Select ENSP00000261590.8:p.His1007Arg
ENST00000261590.12:c.3020A>G (DSG2) ENSP00000261590.8:p.His1007Arg
NM_001943.3:c.3020A>G , LRG_397t1:c.3020A>G (DSG2) NP_001934.2:p.His1007Arg
NR_045216.1:n.1346-500T>C (DSG2-AS1)
NM_001943.4:c.3020A>G (DSG2) NP_001934.2:p.His1007Arg
XM_024451095.1:c.2486A>G (DSG2) XP_024306863.1:p.His829Arg
NM_001943.5:c.3020A>G (DSG2) MANE Select NP_001934.2:p.His1007Arg