Canonical Allele Identifier: CA402146673
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29126116C>G (hg19) chr18:g.31546153C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546153C>G , CM000680.2:g.31546153C>G GRCh38
NC_000018.9:g.29126116C>G , CM000680.1:g.29126116C>G GRCh37
NC_000018.8:g.27380114C>G NCBI36
NG_007072.3:g.52912C>G , LRG_397:g.52912C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2767C>G (DSG2) MANE Select ENSP00000261590.8:p.Pro923Ala
ENST00000261590.12:c.2767C>G (DSG2) ENSP00000261590.8:p.Pro923Ala
NM_001943.3:c.2767C>G , LRG_397t1:c.2767C>G (DSG2) NP_001934.2:p.Pro923Ala
NR_045216.1:n.1346-247G>C (DSG2-AS1)
NM_001943.4:c.2767C>G (DSG2) NP_001934.2:p.Pro923Ala
XM_024451095.1:c.2233C>G (DSG2) XP_024306863.1:p.Pro745Ala
NM_001943.5:c.2767C>G (DSG2) MANE Select NP_001934.2:p.Pro923Ala
Search 100 bp 5'
Search 100 bp 3'