Canonical Allele Identifier: CA618160168
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1295548278
gnomAD v2: 15-59042085-C-T
MyVariant Identifiers: chr15:g.59042085C>T (hg19) chr15:g.58749886C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749886C>T , CM000677.2:g.58749886C>T GRCh38
NC_000015.9:g.59042085C>T , CM000677.1:g.59042085C>T GRCh37
NC_000015.8:g.56829377C>T NCBI36
NG_033876.1:g.5093G>A
NG_033876.2:g.4822G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-352G>A ENSP00000260408.3:n.-352G>A
NM_001110.3:c.-352G>A NP_001101.1:n.-352G>A
NM_001320570.1:c.-352G>A NP_001307499.1:n.-352G>A
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