Canonical Allele Identifier: CA503599172
Gene: DSG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29104524T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524561T>C , CM000680.2:g.31524561T>C GRCh38
NC_000018.9:g.29104524T>C , CM000680.1:g.29104524T>C GRCh37
NC_000018.8:g.27358522T>C NCBI36
NG_007072.3:g.31320T>C , LRG_397:g.31320T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682087.2:n.635T>C
ENST00000683614.2:n.635T>C
ENST00000682087.1:c.635T>C
ENST00000683614.1:c.635T>C
ENST00000261590.13:c.804T>C MANE Select ENSP00000261590.8:p.Asn268=
ENST00000261590.12:c.804T>C ENSP00000261590.8:p.Asn268=
NM_001943.3:c.804T>C , LRG_397t1:c.804T>C NP_001934.2:p.Asn268=
NM_001943.4:c.804T>C NP_001934.2:p.Asn268=
XM_024451095.1:c.270T>C XP_024306863.1:p.Asn90=
NM_001943.5:c.804T>C MANE Select NP_001934.2:p.Asn268=
Search 100 bp 5'
Search 100 bp 3'