Canonical Allele Identifier: CA503596705
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 749713
ClinVar RCV Id: RCV000926617
dbSNP Id: rs1598809953
MyVariant Identifiers: chr18:g.29099783T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31519820T>C , CM000680.2:g.31519820T>C GRCh38
NC_000018.9:g.29099783T>C , CM000680.1:g.29099783T>C GRCh37
NC_000018.8:g.27353781T>C NCBI36
NG_007072.3:g.26579T>C , LRG_397:g.26579T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682241.2:c.99T>C ENSP00000507600.2:p.Asn33=
ENST00000683654.1:c.99T>C ENSP00000506971.1:p.Asn33=
ENST00000261590.13:c.99T>C MANE Select ENSP00000261590.8:p.Asn33=
ENST00000261590.12:c.99T>C ENSP00000261590.8:p.Asn33=
ENST00000585206.1:c.99T>C ENSP00000462503.1:p.Asn33=
NM_001943.3:c.99T>C , LRG_397t1:c.99T>C NP_001934.2:p.Asn33=
NM_001943.4:c.99T>C NP_001934.2:p.Asn33=
XM_024451095.1:c.-436T>C XP_024306863.1:n.-436T>C
NM_001943.5:c.99T>C MANE Select NP_001934.2:p.Asn33=