ClinGen Allele Registry
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Canonical Allele Identifier:
CA15493924
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.42286026G>T
GRCh37
chr7:g.42325625G>T
Linked Data - Sequence & Population
gnomAD v2:
7:42325625 G / T
gnomAD v3:
7:42286026 G / T
gnomAD v4:
chr7-42286026-G-T
Joint Max Group AF
0.13171531 (AMR)
Genomes Max Group AF
0.13171531 (AMR)
Linked Data - NCBI & NCI
dbSNP:
12532960
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.42286026G>T , CM000669.2:g.42286026G>T
GRCh38
NC_000007.13:g.42325625G>T , CM000669.1:g.42325625G>T
GRCh37
NC_000007.12:g.42292150G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'