Canonical Allele Identifier: CA402148774
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070113
ClinVar RCV Id: RCV004010145
MyVariant Identifiers: chr18:g.29126518C>G (hg19) chr18:g.31546555C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546555C>G , CM000680.2:g.31546555C>G GRCh38
NC_000018.9:g.29126518C>G , CM000680.1:g.29126518C>G GRCh37
NC_000018.8:g.27380516C>G NCBI36
NG_007072.3:g.53314C>G , LRG_397:g.53314C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3169C>G (DSG2) MANE Select ENSP00000261590.8:p.Leu1057Val
ENST00000261590.12:c.3169C>G (DSG2) ENSP00000261590.8:p.Leu1057Val
NM_001943.3:c.3169C>G , LRG_397t1:c.3169C>G (DSG2) NP_001934.2:p.Leu1057Val
NR_045216.1:n.1346-649G>C (DSG2-AS1)
NM_001943.4:c.3169C>G (DSG2) NP_001934.2:p.Leu1057Val
XM_024451095.1:c.2635C>G (DSG2) XP_024306863.1:p.Leu879Val
NM_001943.5:c.3169C>G (DSG2) MANE Select NP_001934.2:p.Leu1057Val
Search 100 bp 5'
Search 100 bp 3'