Canonical Allele Identifier: CA271746558

Gene: ADAM10

Linked Data

• dbSNP Id: rs886775779
• gnomAD v2: 15-59042112-C-T
• gnomAD v3: 15-58749913-C-T
• gnomAD v4: 15-58749913-C-T
• MyVariant Identifiers: chr15:g.59042112C>T (hg19) ; chr15:g.58749913C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58749913C>T , CM000677.2:g.58749913C>T	GRCh38
NC_000015.9:g.59042112C>T , CM000677.1:g.59042112C>T	GRCh37
NC_000015.8:g.56829404C>T	NCBI36
NG_033876.1:g.5066G>A
NG_033876.2:g.4795G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.7:c.-379G>A	ENSP00000260408.3:n.-379G>A
NM_001110.3:c.-379G>A	NP_001101.1:n.-379G>A
NM_001320570.1:c.-379G>A	NP_001307499.1:n.-379G>A