Canonical Allele Identifier: CA503765871
Gene: DSG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29111135C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531172C>T , CM000680.2:g.31531172C>T GRCh38
NC_000018.9:g.29111135C>T , CM000680.1:g.29111135C>T GRCh37
NC_000018.8:g.27365133C>T NCBI36
NG_007072.3:g.37931C>T , LRG_397:g.37931C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000683614.2:n.1031C>T
ENST00000683614.1:c.1031C>T
ENST00000261590.13:c.1200C>T MANE Select ENSP00000261590.8:p.Ser400=
ENST00000261590.12:c.1200C>T ENSP00000261590.8:p.Ser400=
NM_001943.3:c.1200C>T , LRG_397t1:c.1200C>T NP_001934.2:p.Ser400=
NM_001943.4:c.1200C>T NP_001934.2:p.Ser400=
XM_024451095.1:c.666C>T XP_024306863.1:p.Ser222=
NM_001943.5:c.1200C>T MANE Select NP_001934.2:p.Ser400=