ClinGen Allele Registry
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Canonical Allele Identifier:
CA166742016
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.128241090C>A
GRCh37
chr7:g.127881143C>A
Linked Data - Sequence & Population
gnomAD v2:
7:127881143 C / A
gnomAD v3:
7:128241090 C / A
gnomAD v4:
chr7-128241090-C-A
Joint Max Group AF
0.1147815 (AFR)
Genomes Max Group AF
0.1147815 (AFR)
Linked Data - NCBI & NCI
dbSNP:
791620
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.128241090C>A , CM000669.2:g.128241090C>A
GRCh38
NC_000007.13:g.127881143C>A , CM000669.1:g.127881143C>A
GRCh37
NC_000007.12:g.127668379C>A
NCBI36
NG_007450.1:g.4813C>A
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