Canonical Allele Identifier: CA2180493175
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1899930478

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749918G>C , CM000677.2:g.58749918G>C GRCh38
NC_000015.9:g.59042117G>C , CM000677.1:g.59042117G>C GRCh37
NC_000015.8:g.56829409G>C NCBI36
NG_033876.1:g.5061C>G
NG_033876.2:g.4790C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-384C>G ENSP00000260408.3:n.-384C>G
NM_001110.3:c.-384C>G NP_001101.1:n.-384C>G
NM_001320570.1:c.-384C>G NP_001307499.1:n.-384C>G