Canonical Allele Identifier: CA2180493275
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1595679151
gnomAD v4: 15-58749953-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749953T>C , CM000677.2:g.58749953T>C GRCh38
NC_000015.9:g.59042152T>C , CM000677.1:g.59042152T>C GRCh37
NC_000015.8:g.56829444T>C NCBI36
NG_033876.1:g.5026A>G
NG_033876.2:g.4755A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-419A>G ENSP00000260408.3:n.-419A>G
NM_001110.3:c.-419A>G NP_001101.1:n.-419A>G
NM_001320570.1:c.-419A>G NP_001307499.1:n.-419A>G
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