Canonical Allele Identifier: CA503766491
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29126298T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546335T>A , CM000680.2:g.31546335T>A GRCh38
NC_000018.9:g.29126298T>A , CM000680.1:g.29126298T>A GRCh37
NC_000018.8:g.27380296T>A NCBI36
NG_007072.3:g.53094T>A , LRG_397:g.53094T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.2949T>A (DSG2) MANE Select ENSP00000261590.8:p.Gly983=
ENST00000261590.12:c.2949T>A (DSG2) ENSP00000261590.8:p.Gly983=
NM_001943.3:c.2949T>A , LRG_397t1:c.2949T>A (DSG2) NP_001934.2:p.Gly983=
NR_045216.1:n.1346-429A>T (DSG2-AS1)
NM_001943.4:c.2949T>A (DSG2) NP_001934.2:p.Gly983=
XM_024451095.1:c.2415T>A (DSG2) XP_024306863.1:p.Gly805=
NM_001943.5:c.2949T>A (DSG2) MANE Select NP_001934.2:p.Gly983=