Canonical Allele Identifier: CA2641405662
Gene: DSG2 HGNC NCBI

Linked Data

gnomAD v4: 18-31498222-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498222G>A , CM000680.2:g.31498222G>A GRCh38
NC_000018.9:g.29078185G>A , CM000680.1:g.29078185G>A GRCh37
NC_000018.8:g.27332183G>A NCBI36
NG_007072.3:g.4981G>A , LRG_397:g.4981G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682241.2:c.-30G>A ENSP00000507600.2:n.-30G>A
ENST00000261590.13:c.-30G>A MANE Select ENSP00000261590.8:n.-30G>A
ENST00000261590.12:c.-30G>A ENSP00000261590.8:n.-30G>A
ENST00000585206.1:c.-30G>A ENSP00000462503.1:n.-30G>A
NM_001943.3:c.-30G>A , LRG_397t1:c.-30G>A NP_001934.2:n.-30G>A
NM_001943.4:c.-30G>A NP_001934.2:n.-30G>A
NM_001943.5:c.-30G>A MANE Select NP_001934.2:n.-30G>A
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