ClinGen Allele Registry
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Canonical Allele Identifier:
CA11471231
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.39263303C>T
GRCh37
chr3:g.39304794C>T
Linked Data - Sequence & Population
gnomAD v2:
3:39304794 C / T
gnomAD v3:
3:39263303 C / T
gnomAD v4:
chr3-39263303-C-T
Joint Max Group AF
0.38669128 (MID)
Genomes Max Group AF
0.35357159 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11129820
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.39263303C>T , CM000665.2:g.39263303C>T
GRCh38
NC_000003.11:g.39304794C>T , CM000665.1:g.39304794C>T
GRCh37
NC_000003.10:g.39279798C>T
NCBI36
NG_016362.1:g.23433G>A
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