Canonical Allele Identifier: CA2293866866
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1598828870

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547810C>T , CM000680.2:g.31547810C>T GRCh38
NC_000018.9:g.29127773C>T , CM000680.1:g.29127773C>T GRCh37
NC_000018.8:g.27381771C>T NCBI36
NG_007072.3:g.54569C>T , LRG_397:g.54569C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*1067C>T (DSG2) MANE Select ENSP00000261590.8:n.*1067C>T
ENST00000261590.12:c.*1067C>T (DSG2) ENSP00000261590.8:n.*1067C>T
NM_001943.3:c.*1067C>T , LRG_397t1:c.*1067C>T (DSG2) NP_001934.2:n.*1067C>T
NR_045216.1:n.1346-1904G>A (DSG2-AS1)
NM_001943.4:c.*1067C>T (DSG2) NP_001934.2:n.*1067C>T
NM_001943.5:c.*1067C>T (DSG2) MANE Select NP_001934.2:n.*1067C>T