Canonical Allele Identifier: CA271746598

Gene: ADAM10

Linked Data

• dbSNP Id: rs55744618
• gnomAD v2: 15-59042155-C-T
• gnomAD v3: 15-58749956-C-T
• gnomAD v4: 15-58749956-C-T
• MyVariant Identifiers: chr15:g.59042155C>T (hg19) ; chr15:g.58749956C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58749956C>T , CM000677.2:g.58749956C>T	GRCh38
NC_000015.9:g.59042155C>T , CM000677.1:g.59042155C>T	GRCh37
NC_000015.8:g.56829447C>T	NCBI36
NG_033876.1:g.5023G>A
NG_033876.2:g.4752G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.7:c.-422G>A	ENSP00000260408.3:n.-422G>A
NM_001110.3:c.-422G>A	NP_001101.1:n.-422G>A
NM_001320570.1:c.-422G>A	NP_001307499.1:n.-422G>A