Canonical Allele Identifier: CA271746544
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs199972921
gnomAD v2: 15-59042095-C-T
gnomAD v3: 15-58749896-C-T
gnomAD v4: 15-58749896-C-T
MyVariant Identifiers: chr15:g.59042095C>T (hg19) chr15:g.58749896C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749896C>T , CM000677.2:g.58749896C>T GRCh38
NC_000015.9:g.59042095C>T , CM000677.1:g.59042095C>T GRCh37
NC_000015.8:g.56829387C>T NCBI36
NG_033876.1:g.5083G>A
NG_033876.2:g.4812G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-362G>A ENSP00000260408.3:n.-362G>A
NM_001110.3:c.-362G>A NP_001101.1:n.-362G>A
NM_001320570.1:c.-362G>A NP_001307499.1:n.-362G>A
Search 100 bp 5'
Search 100 bp 3'