Canonical Allele Identifier: CA044887
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 920612
ClinVar RCV Id: RCV001179462 RCV001361742
dbSNP Id: rs759420598
ExAC: 18:29122592 T / C
gnomAD v2: 18-29122592-T-C
gnomAD v4: 18-31542629-T-C
MyVariant Identifiers: chr18:g.29122592T>C (hg19) chr18:g.31542629T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542629T>C , CM000680.2:g.31542629T>C GRCh38
NC_000018.9:g.29122592T>C , CM000680.1:g.29122592T>C GRCh37
NC_000018.8:g.27376590T>C NCBI36
NG_007072.3:g.49388T>C , LRG_397:g.49388T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2111T>C (DSG2) MANE Select ENSP00000261590.8:p.Ile704Thr
ENST00000261590.12:c.2111T>C (DSG2) ENSP00000261590.8:p.Ile704Thr
NM_001943.3:c.2111T>C , LRG_397t1:c.2111T>C (DSG2) NP_001934.2:p.Ile704Thr
NR_045216.1:n.1811-308A>G (DSG2-AS1)
NM_001943.4:c.2111T>C (DSG2) NP_001934.2:p.Ile704Thr
XM_024451095.1:c.1577T>C (DSG2) XP_024306863.1:p.Ile526Thr
NM_001943.5:c.2111T>C (DSG2) MANE Select NP_001934.2:p.Ile704Thr
Search 100 bp 5'
Search 100 bp 3'