ClinGen Allele Registry
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Canonical Allele Identifier:
CA11752959
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.67756760G>A
GRCh37
chr4:g.68622478G>A
Linked Data - Sequence & Population
gnomAD v2:
4:68622478 G / A
gnomAD v3:
4:67756760 G / A
gnomAD v4:
chr4-67756760-G-A
Joint Max Group AF
0.55174121 (SAS)
Genomes Max Group AF
0.55174121 (SAS)
Linked Data - NCBI & NCI
dbSNP:
3756159
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.67756760G>A , CM000666.2:g.67756760G>A
GRCh38
NC_000004.11:g.68622478G>A , CM000666.1:g.68622478G>A
GRCh37
NC_000004.10:g.68305073G>A
NCBI36
NG_009293.1:g.4327C>T
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