Canonical Allele Identifier: CA297702700
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1042667056
gnomAD v2: 18-29126646-C-T
gnomAD v4: 18-31546683-C-T
MyVariant Identifiers: chr18:g.29126646C>T (hg19) chr18:g.31546683C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546683C>T , CM000680.2:g.31546683C>T GRCh38
NC_000018.9:g.29126646C>T , CM000680.1:g.29126646C>T GRCh37
NC_000018.8:g.27380644C>T NCBI36
NG_007072.3:g.53442C>T , LRG_397:g.53442C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3297C>T (DSG2) MANE Select ENSP00000261590.8:p.Thr1099=
ENST00000261590.12:c.3297C>T (DSG2) ENSP00000261590.8:p.Thr1099=
NM_001943.3:c.3297C>T , LRG_397t1:c.3297C>T (DSG2) NP_001934.2:p.Thr1099=
NR_045216.1:n.1346-777G>A (DSG2-AS1)
NM_001943.4:c.3297C>T (DSG2) NP_001934.2:p.Thr1099=
XM_024451095.1:c.2763C>T (DSG2) XP_024306863.1:p.Thr921=
NM_001943.5:c.3297C>T (DSG2) MANE Select NP_001934.2:p.Thr1099=
Search 100 bp 5'
Search 100 bp 3'