Canonical Allele Identifier: CA2180493067
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1294114480

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749884G>A , CM000677.2:g.58749884G>A GRCh38
NC_000015.9:g.59042083G>A , CM000677.1:g.59042083G>A GRCh37
NC_000015.8:g.56829375G>A NCBI36
NG_033876.1:g.5095C>T
NG_033876.2:g.4824C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-350C>T ENSP00000260408.3:n.-350C>T
NM_001110.3:c.-350C>T NP_001101.1:n.-350C>T
NM_001320570.1:c.-350C>T NP_001307499.1:n.-350C>T