ClinGen Allele Registry
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Canonical Allele Identifier:
CA116258035
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.27611324G>T
GRCh37
chr5:g.27611431G>T
Linked Data - Sequence & Population
gnomAD v2:
5:27611431 G / T
gnomAD v3:
5:27611324 G / T
gnomAD v4:
chr5-27611324-G-T
Joint Max Group AF
0.67774951 (EAS)
Genomes Max Group AF
0.67774951 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12054895
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.27611324G>T , CM000667.2:g.27611324G>T
GRCh38
NC_000005.9:g.27611431G>T , CM000667.1:g.27611431G>T
GRCh37
NC_000005.8:g.27647188G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'