Canonical Allele Identifier: CA402148785
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29126521C>G (hg19) chr18:g.31546558C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546558C>G , CM000680.2:g.31546558C>G GRCh38
NC_000018.9:g.29126521C>G , CM000680.1:g.29126521C>G GRCh37
NC_000018.8:g.27380519C>G NCBI36
NG_007072.3:g.53317C>G , LRG_397:g.53317C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3172C>G (DSG2) MANE Select ENSP00000261590.8:p.Gln1058Glu
ENST00000261590.12:c.3172C>G (DSG2) ENSP00000261590.8:p.Gln1058Glu
NM_001943.3:c.3172C>G , LRG_397t1:c.3172C>G (DSG2) NP_001934.2:p.Gln1058Glu
NR_045216.1:n.1346-652G>C (DSG2-AS1)
NM_001943.4:c.3172C>G (DSG2) NP_001934.2:p.Gln1058Glu
XM_024451095.1:c.2638C>G (DSG2) XP_024306863.1:p.Gln880Glu
NM_001943.5:c.3172C>G (DSG2) MANE Select NP_001934.2:p.Gln1058Glu
Search 100 bp 5'
Search 100 bp 3'