Canonical Allele Identifier: CA10576166
Gene:
MyVariant.info:
GRCh38 chr10:g.94645745G>A
GRCh37 chr10:g.96405502G>A
gnomAD v2:
10:96405502 G / A
gnomAD v3:
10:94645745 G / A
gnomAD v4:
chr10-94645745-G-A
Joint Max Group AF 0.32092052 (SAS)
Genomes Max Group AF 0.32092052 (SAS)
ClinVar RCV:
RCV000211190
ClinVar Variation:
225947
dbSNP:
12777823
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94645745G>A , CM000672.2:g.94645745G>A GRCh38
NC_000010.10:g.96405502G>A , CM000672.1:g.96405502G>A GRCh37
NC_000010.9:g.96395492G>A NCBI36
Search 100 bp 5'
Search 100 bp 3'