Canonical Allele Identifier: CA14082373
Gene: ADAM10 HGNC NCBI
MyVariant.info:
GRCh38 chr15:g.58749813T>C
GRCh37 chr15:g.59042012T>C
gnomAD v2:
15:59042012 T / C
gnomAD v3:
15:58749813 T / C
gnomAD v4:
chr15-58749813-T-C
Joint Max Group AF 0.85378877 (EAS)
Genomes Max Group AF 0.8187602 (EAS)
Exomes Max Group AF 0.8572539 (EAS)
ClinVar RCV:
RCV001669363
ClinVar Variation:
1260546
dbSNP:
653765
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749813T>C , CM000677.2:g.58749813T>C GRCh38
NC_000015.9:g.59042012T>C , CM000677.1:g.59042012T>C GRCh37
NC_000015.8:g.56829304T>C NCBI36
NG_033876.1:g.5166A>G
NG_033876.2:g.4895A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-279A>G ENSP00000260408.3:n.-279A>G
NM_001110.3:c.-279A>G NP_001101.1:n.-279A>G
NM_001320570.1:c.-279A>G NP_001307499.1:n.-279A>G
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