Canonical Allele Identifier: CA618160171

Gene: ADAM10

Linked Data

• dbSNP Id: rs999481918
• gnomAD v2: 15-59042121-C-G
• gnomAD v3: 15-58749922-C-G
• gnomAD v4: 15-58749922-C-G
• MyVariant Identifiers: chr15:g.59042121C>G (hg19) ; chr15:g.58749922C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58749922C>G , CM000677.2:g.58749922C>G	GRCh38
NC_000015.9:g.59042121C>G , CM000677.1:g.59042121C>G	GRCh37
NC_000015.8:g.56829413C>G	NCBI36
NG_033876.1:g.5057G>C
NG_033876.2:g.4786G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.7:c.-388G>C	ENSP00000260408.3:n.-388G>C
NM_001110.3:c.-388G>C	NP_001101.1:n.-388G>C
NM_001320570.1:c.-388G>C	NP_001307499.1:n.-388G>C