Canonical Allele Identifier: CA778427200
Gene: DSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1290208365

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498071C>T , CM000680.2:g.31498071C>T GRCh38
NC_000018.9:g.29078034C>T , CM000680.1:g.29078034C>T GRCh37
NC_000018.8:g.27332032C>T NCBI36
NG_007072.3:g.4830C>T , LRG_397:g.4830C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.12:c.-181C>T ENSP00000261590.8:n.-181C>T
NM_001943.3:c.-181C>T , LRG_397t1:c.-181C>T NP_001934.2:n.-181C>T
NM_001943.4:c.-181C>T NP_001934.2:n.-181C>T