ClinGen Allele Registry
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Canonical Allele Identifier:
CA13059024
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.129812583C>T
GRCh37
chr9:g.132574862C>T
Linked Data - Sequence & Population
gnomAD v2:
9:132574862 C / T
gnomAD v3:
9:129812583 C / T
gnomAD v4:
chr9-129812583-C-T
Joint Max Group AF
0.23353012 (NFE)
Genomes Max Group AF
0.23353012 (NFE)
Linked Data - NCBI & NCI
dbSNP:
13283584
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.129812583C>T , CM000671.2:g.129812583C>T
GRCh38
NC_000009.11:g.132574862C>T , CM000671.1:g.132574862C>T
GRCh37
NC_000009.10:g.131614683C>T
NCBI36
NG_008049.1:g.16580G>A
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