Canonical Allele Identifier: CA402127528
Gene: DSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1021457619
gnomAD v4: 18-31498254-G-C
MyVariant Identifiers: chr18:g.29078217G>C (hg19) chr18:g.31498254G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498254G>C , CM000680.2:g.31498254G>C GRCh38
NC_000018.9:g.29078217G>C , CM000680.1:g.29078217G>C GRCh37
NC_000018.8:g.27332215G>C NCBI36
NG_007072.3:g.5013G>C , LRG_397:g.5013G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682241.2:c.3G>C ENSP00000507600.2:p.Met1Ile
ENST00000683654.1:c.3G>C ENSP00000506971.1:p.Met1Ile
ENST00000261590.13:c.3G>C MANE Select ENSP00000261590.8:p.Met1Ile
ENST00000261590.12:c.3G>C ENSP00000261590.8:p.Met1Ile
ENST00000585206.1:c.3G>C ENSP00000462503.1:p.Met1Ile
NM_001943.3:c.3G>C , LRG_397t1:c.3G>C NP_001934.2:p.Met1Ile
NM_001943.4:c.3G>C NP_001934.2:p.Met1Ile
NM_001943.5:c.3G>C MANE Select NP_001934.2:p.Met1Ile
Search 100 bp 5'
Search 100 bp 3'