ClinGen Allele Registry
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Canonical Allele Identifier:
CA12962746
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.91213189G>A
GRCh37
chr9:g.93975471G>A
Linked Data - Sequence & Population
gnomAD v2:
9:93975471 G / A
gnomAD v3:
9:91213189 G / A
gnomAD v4:
chr9-91213189-G-A
Joint Max Group AF
0.63764238 (NFE)
Genomes Max Group AF
0.63764238 (NFE)
Linked Data - NCBI & NCI
dbSNP:
773506
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.91213189G>A , CM000671.2:g.91213189G>A
GRCh38
NC_000009.11:g.93975471G>A , CM000671.1:g.93975471G>A
GRCh37
NC_000009.10:g.93015292G>A
NCBI36
NG_008017.1:g.153736C>T , LRG_449:g.153736C>T
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