Canonical Allele Identifier: CA2731086909
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs2140860731

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749931G>C , CM000677.2:g.58749931G>C GRCh38
NC_000015.9:g.59042130G>C , CM000677.1:g.59042130G>C GRCh37
NC_000015.8:g.56829422G>C NCBI36
NG_033876.1:g.5048C>G
NG_033876.2:g.4777C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-397C>G ENSP00000260408.3:n.-397C>G
NM_001110.3:c.-397C>G NP_001101.1:n.-397C>G
NM_001320570.1:c.-397C>G NP_001307499.1:n.-397C>G