Canonical Allele Identifier: CA402139956
Gene: DSG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29121273A>G (hg19) chr18:g.31541310A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31541310A>G , CM000680.2:g.31541310A>G GRCh38
NC_000018.9:g.29121273A>G , CM000680.1:g.29121273A>G GRCh37
NC_000018.8:g.27375271A>G NCBI36
NG_007072.3:g.48069A>G , LRG_397:g.48069A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1997A>G MANE Select ENSP00000261590.8:p.Asp666Gly
ENST00000261590.12:c.1997A>G ENSP00000261590.8:p.Asp666Gly
NM_001943.3:c.1997A>G , LRG_397t1:c.1997A>G NP_001934.2:p.Asp666Gly
NM_001943.4:c.1997A>G NP_001934.2:p.Asp666Gly
XM_024451095.1:c.1463A>G XP_024306863.1:p.Asp488Gly
NM_001943.5:c.1997A>G MANE Select NP_001934.2:p.Asp666Gly
Search 100 bp 5'
Search 100 bp 3'