Canonical Allele Identifier: CA402139838
Gene: DSG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29121257G>C (hg19) chr18:g.31541294G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31541294G>C , CM000680.2:g.31541294G>C GRCh38
NC_000018.9:g.29121257G>C , CM000680.1:g.29121257G>C GRCh37
NC_000018.8:g.27375255G>C NCBI36
NG_007072.3:g.48053G>C , LRG_397:g.48053G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.1981G>C MANE Select ENSP00000261590.8:p.Gly661Arg
ENST00000261590.12:c.1981G>C ENSP00000261590.8:p.Gly661Arg
NM_001943.3:c.1981G>C , LRG_397t1:c.1981G>C NP_001934.2:p.Gly661Arg
NM_001943.4:c.1981G>C NP_001934.2:p.Gly661Arg
XM_024451095.1:c.1447G>C XP_024306863.1:p.Gly483Arg
NM_001943.5:c.1981G>C MANE Select NP_001934.2:p.Gly661Arg
Search 100 bp 5'
Search 100 bp 3'