ClinGen Allele Registry
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Canonical Allele Identifier:
CA15618101
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.29592838G>T
GRCh37
chr9:g.29592836G>T
Linked Data - Sequence & Population
gnomAD v2:
9:29592836 G / T
gnomAD v3:
9:29592838 G / T
gnomAD v4:
chr9-29592838-G-T
Joint Max Group AF
0.51499021 (NFE)
Genomes Max Group AF
0.51499021 (NFE)
Linked Data - NCBI & NCI
dbSNP:
560764
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.29592838G>T , CM000671.2:g.29592838G>T
GRCh38
NC_000009.11:g.29592836G>T , CM000671.1:g.29592836G>T
GRCh37
NC_000009.10:g.29582836G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'