Canonical Allele Identifier: CA970326878
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1170587960
gnomAD v3: 15-58749950-G-A
gnomAD v4: 15-58749950-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749950G>A , CM000677.2:g.58749950G>A GRCh38
NC_000015.9:g.59042149G>A , CM000677.1:g.59042149G>A GRCh37
NC_000015.8:g.56829441G>A NCBI36
NG_033876.1:g.5029C>T
NG_033876.2:g.4758C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-416C>T ENSP00000260408.3:n.-416C>T
NM_001110.3:c.-416C>T NP_001101.1:n.-416C>T
NM_001320570.1:c.-416C>T NP_001307499.1:n.-416C>T
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