Canonical Allele Identifier: CA714361134
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1418521632
gnomAD v4: 15-58749970-T-G
MyVariant Identifiers: chr15:g.59042169T>G (hg19) chr15:g.58749970T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749970T>G , CM000677.2:g.58749970T>G GRCh38
NC_000015.9:g.59042169T>G , CM000677.1:g.59042169T>G GRCh37
NC_000015.8:g.56829461T>G NCBI36
NG_033876.1:g.5009A>C
NG_033876.2:g.4738A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-436A>C ENSP00000260408.3:n.-436A>C
NM_001110.3:c.-436A>C NP_001101.1:n.-436A>C
NM_001320570.1:c.-436A>C NP_001307499.1:n.-436A>C
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