Canonical Allele Identifier: CA503766313
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29126094G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546131G>A , CM000680.2:g.31546131G>A GRCh38
NC_000018.9:g.29126094G>A , CM000680.1:g.29126094G>A GRCh37
NC_000018.8:g.27380092G>A NCBI36
NG_007072.3:g.52890G>A , LRG_397:g.52890G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2745G>A (DSG2) MANE Select ENSP00000261590.8:p.Arg915=
ENST00000261590.12:c.2745G>A (DSG2) ENSP00000261590.8:p.Arg915=
NM_001943.3:c.2745G>A , LRG_397t1:c.2745G>A (DSG2) NP_001934.2:p.Arg915=
NR_045216.1:n.1346-225C>T (DSG2-AS1)
NM_001943.4:c.2745G>A (DSG2) NP_001934.2:p.Arg915=
XM_024451095.1:c.2211G>A (DSG2) XP_024306863.1:p.Arg737=
NM_001943.5:c.2745G>A (DSG2) MANE Select NP_001934.2:p.Arg915=
Search 100 bp 5'
Search 100 bp 3'