Canonical Allele Identifier: CA2180493101
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1899929418
gnomAD v4: 15-58749902-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749902T>C , CM000677.2:g.58749902T>C GRCh38
NC_000015.9:g.59042101T>C , CM000677.1:g.59042101T>C GRCh37
NC_000015.8:g.56829393T>C NCBI36
NG_033876.1:g.5077A>G
NG_033876.2:g.4806A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-368A>G ENSP00000260408.3:n.-368A>G
NM_001110.3:c.-368A>G NP_001101.1:n.-368A>G
NM_001320570.1:c.-368A>G NP_001307499.1:n.-368A>G
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