Canonical Allele Identifier: CA2628693598
Gene: ADAM10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749883C>A , CM000677.2:g.58749883C>A GRCh38
NC_000015.9:g.59042082C>A , CM000677.1:g.59042082C>A GRCh37
NC_000015.8:g.56829374C>A NCBI36
NG_033876.1:g.5096G>T
NG_033876.2:g.4825G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-349G>T ENSP00000260408.3:n.-349G>T
NM_001110.3:c.-349G>T NP_001101.1:n.-349G>T
NM_001320570.1:c.-349G>T NP_001307499.1:n.-349G>T