ClinGen Allele Registry
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Canonical Allele Identifier:
CA23507908
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.67260421T>C
GRCh37
chr1:g.67726104T>C
Linked Data - Sequence & Population
gnomAD v2:
1:67726104 T / C
gnomAD v3:
1:67260421 T / C
gnomAD v4:
chr1-67260421-T-C
Joint Max Group AF
0.27986014 (AFR)
Genomes Max Group AF
0.27986014 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9988642
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.67260421T>C , CM000663.2:g.67260421T>C
GRCh38
NC_000001.10:g.67726104T>C , CM000663.1:g.67726104T>C
GRCh37
NC_000001.9:g.67498692T>C
NCBI36
NG_011498.1:g.98936T>C
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