Canonical Allele Identifier: CA503599260
Gene: DSG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29104713C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524750C>A , CM000680.2:g.31524750C>A GRCh38
NC_000018.9:g.29104713C>A , CM000680.1:g.29104713C>A GRCh37
NC_000018.8:g.27358711C>A NCBI36
NG_007072.3:g.31509C>A , LRG_397:g.31509C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682087.2:n.707C>A
ENST00000683614.2:n.707C>A
ENST00000682087.1:c.707C>A
ENST00000683614.1:c.707C>A
ENST00000261590.13:c.876C>A MANE Select ENSP00000261590.8:p.Arg292=
ENST00000261590.12:c.876C>A ENSP00000261590.8:p.Arg292=
NM_001943.3:c.876C>A , LRG_397t1:c.876C>A NP_001934.2:p.Arg292=
NM_001943.4:c.876C>A NP_001934.2:p.Arg292=
XM_024451095.1:c.342C>A XP_024306863.1:p.Arg114=
NM_001943.5:c.876C>A MANE Select NP_001934.2:p.Arg292=
Search 100 bp 5'
Search 100 bp 3'