Canonical Allele Identifier: CA2641405508
Gene: DSG2 HGNC NCBI

Linked Data

gnomAD v4: 18-31498111-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498111A>T , CM000680.2:g.31498111A>T GRCh38
NC_000018.9:g.29078074A>T , CM000680.1:g.29078074A>T GRCh37
NC_000018.8:g.27332072A>T NCBI36
NG_007072.3:g.4870A>T , LRG_397:g.4870A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.12:c.-141A>T ENSP00000261590.8:n.-141A>T
NM_001943.3:c.-141A>T , LRG_397t1:c.-141A>T NP_001934.2:n.-141A>T
NM_001943.4:c.-141A>T NP_001934.2:n.-141A>T
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