Canonical Allele Identifier: CA2180493329
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs756740287
gnomAD v4: 15-58749976-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749976C>A , CM000677.2:g.58749976C>A GRCh38
NC_000015.9:g.59042175C>A , CM000677.1:g.59042175C>A GRCh37
NC_000015.8:g.56829467C>A NCBI36
NG_033876.1:g.5003G>T
NG_033876.2:g.4732G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-442G>T ENSP00000260408.3:n.-442G>T
NM_001110.3:c.-442G>T NP_001101.1:n.-442G>T
NM_001320570.1:c.-442G>T NP_001307499.1:n.-442G>T
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