Canonical Allele Identifier: CA714361096
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1459601635
gnomAD v3: 15-58749949-C-A
gnomAD v4: 15-58749949-C-A
MyVariant Identifiers: chr15:g.59042148C>A (hg19) chr15:g.58749949C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749949C>A , CM000677.2:g.58749949C>A GRCh38
NC_000015.9:g.59042148C>A , CM000677.1:g.59042148C>A GRCh37
NC_000015.8:g.56829440C>A NCBI36
NG_033876.1:g.5030G>T
NG_033876.2:g.4759G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-415G>T ENSP00000260408.3:n.-415G>T
NM_001110.3:c.-415G>T NP_001101.1:n.-415G>T
NM_001320570.1:c.-415G>T NP_001307499.1:n.-415G>T
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