Canonical Allele Identifier: CA714361053

Gene: ADAM10

Linked Data

• dbSNP Id: rs1229808733
• gnomAD v3: 15-58749909-C-G
• gnomAD v4: 15-58749909-C-G
• MyVariant Identifiers: chr15:g.59042108C>G (hg19) ; chr15:g.58749909C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58749909C>G , CM000677.2:g.58749909C>G	GRCh38
NC_000015.9:g.59042108C>G , CM000677.1:g.59042108C>G	GRCh37
NC_000015.8:g.56829400C>G	NCBI36
NG_033876.1:g.5070G>C
NG_033876.2:g.4799G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.7:c.-375G>C	ENSP00000260408.3:n.-375G>C
NM_001110.3:c.-375G>C	NP_001101.1:n.-375G>C
NM_001320570.1:c.-375G>C	NP_001307499.1:n.-375G>C