Canonical Allele Identifier: CA402148432
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1293745476
MyVariant Identifiers: chr18:g.29126452A>G (hg19) chr18:g.31546489A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546489A>G , CM000680.2:g.31546489A>G GRCh38
NC_000018.9:g.29126452A>G , CM000680.1:g.29126452A>G GRCh37
NC_000018.8:g.27380450A>G NCBI36
NG_007072.3:g.53248A>G , LRG_397:g.53248A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.3103A>G (DSG2) MANE Select ENSP00000261590.8:p.Met1035Val
ENST00000261590.12:c.3103A>G (DSG2) ENSP00000261590.8:p.Met1035Val
NM_001943.3:c.3103A>G , LRG_397t1:c.3103A>G (DSG2) NP_001934.2:p.Met1035Val
NR_045216.1:n.1346-583T>C (DSG2-AS1)
NM_001943.4:c.3103A>G (DSG2) NP_001934.2:p.Met1035Val
XM_024451095.1:c.2569A>G (DSG2) XP_024306863.1:p.Met857Val
NM_001943.5:c.3103A>G (DSG2) MANE Select NP_001934.2:p.Met1035Val
Search 100 bp 5'
Search 100 bp 3'