Canonical Allele Identifier: CA714361116
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1205365785
gnomAD v3: 15-58749965-A-G
gnomAD v4: 15-58749965-A-G
MyVariant Identifiers: chr15:g.59042164A>G (hg19) chr15:g.58749965A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749965A>G , CM000677.2:g.58749965A>G GRCh38
NC_000015.9:g.59042164A>G , CM000677.1:g.59042164A>G GRCh37
NC_000015.8:g.56829456A>G NCBI36
NG_033876.1:g.5014T>C
NG_033876.2:g.4743T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-431T>C ENSP00000260408.3:n.-431T>C
NM_001110.3:c.-431T>C NP_001101.1:n.-431T>C
NM_001320570.1:c.-431T>C NP_001307499.1:n.-431T>C
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