Canonical Allele Identifier: CA2180493081
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1899928968

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749890A>G , CM000677.2:g.58749890A>G GRCh38
NC_000015.9:g.59042089A>G , CM000677.1:g.59042089A>G GRCh37
NC_000015.8:g.56829381A>G NCBI36
NG_033876.1:g.5089T>C
NG_033876.2:g.4818T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-356T>C ENSP00000260408.3:n.-356T>C
NM_001110.3:c.-356T>C NP_001101.1:n.-356T>C
NM_001320570.1:c.-356T>C NP_001307499.1:n.-356T>C