Canonical Allele Identifier: CA2180493074
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1899928891
gnomAD v4: 15-58749887-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749887C>T , CM000677.2:g.58749887C>T GRCh38
NC_000015.9:g.59042086C>T , CM000677.1:g.59042086C>T GRCh37
NC_000015.8:g.56829378C>T NCBI36
NG_033876.1:g.5092G>A
NG_033876.2:g.4821G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-353G>A ENSP00000260408.3:n.-353G>A
NM_001110.3:c.-353G>A NP_001101.1:n.-353G>A
NM_001320570.1:c.-353G>A NP_001307499.1:n.-353G>A
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