Canonical Allele Identifier: CA503766396
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29126214T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546251T>C , CM000680.2:g.31546251T>C GRCh38
NC_000018.9:g.29126214T>C , CM000680.1:g.29126214T>C GRCh37
NC_000018.8:g.27380212T>C NCBI36
NG_007072.3:g.53010T>C , LRG_397:g.53010T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.2865T>C (DSG2) MANE Select ENSP00000261590.8:p.Pro955=
ENST00000261590.12:c.2865T>C (DSG2) ENSP00000261590.8:p.Pro955=
NM_001943.3:c.2865T>C , LRG_397t1:c.2865T>C (DSG2) NP_001934.2:p.Pro955=
NR_045216.1:n.1346-345A>G (DSG2-AS1)
NM_001943.4:c.2865T>C (DSG2) NP_001934.2:p.Pro955=
XM_024451095.1:c.2331T>C (DSG2) XP_024306863.1:p.Pro777=
NM_001943.5:c.2865T>C (DSG2) MANE Select NP_001934.2:p.Pro955=
Search 100 bp 5'
Search 100 bp 3'