Canonical Allele Identifier: CA048270
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 386199
ClinVar RCV Id: RCV000439043 RCV000864990 RCV001184547 RCV002446703 RCV004000448
dbSNP Id: rs757473850
ExAC: 18:29126640 T / C
gnomAD v2: 18-29126640-T-C
gnomAD v3: 18-31546677-T-C
gnomAD v4: 18-31546677-T-C
MyVariant Identifiers: chr18:g.29126640T>C (hg19) chr18:g.31546677T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546677T>C , CM000680.2:g.31546677T>C GRCh38
NC_000018.9:g.29126640T>C , CM000680.1:g.29126640T>C GRCh37
NC_000018.8:g.27380638T>C NCBI36
NG_007072.3:g.53436T>C , LRG_397:g.53436T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3291T>C (DSG2) MANE Select ENSP00000261590.8:p.Asn1097=
ENST00000261590.12:c.3291T>C (DSG2) ENSP00000261590.8:p.Asn1097=
NM_001943.3:c.3291T>C , LRG_397t1:c.3291T>C (DSG2) NP_001934.2:p.Asn1097=
NR_045216.1:n.1346-771A>G (DSG2-AS1)
NM_001943.4:c.3291T>C (DSG2) NP_001934.2:p.Asn1097=
XM_024451095.1:c.2757T>C (DSG2) XP_024306863.1:p.Asn919=
NM_001943.5:c.3291T>C (DSG2) MANE Select NP_001934.2:p.Asn1097=
Search 100 bp 5'
Search 100 bp 3'