Canonical Allele Identifier: CA2180493189
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1899930628

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749920T>C , CM000677.2:g.58749920T>C GRCh38
NC_000015.9:g.59042119T>C , CM000677.1:g.59042119T>C GRCh37
NC_000015.8:g.56829411T>C NCBI36
NG_033876.1:g.5059A>G
NG_033876.2:g.4788A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-386A>G ENSP00000260408.3:n.-386A>G
NM_001110.3:c.-386A>G NP_001101.1:n.-386A>G
NM_001320570.1:c.-386A>G NP_001307499.1:n.-386A>G