ClinGen Allele Registry
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Canonical Allele Identifier:
CA31389808
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.159711574G>C
GRCh37
chr1:g.159681364G>C
Linked Data - Sequence & Population
gnomAD v2:
1:159681364 G / C
gnomAD v3:
1:159711574 G / C
gnomAD v4:
chr1-159711574-G-C
Joint Max Group AF
0.26425867 (AFR)
Genomes Max Group AF
0.26425867 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3093068
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.159711574G>C , CM000663.2:g.159711574G>C
GRCh38
NC_000001.10:g.159681364G>C , CM000663.1:g.159681364G>C
GRCh37
NC_000001.9:g.157947988G>C
NCBI36
NG_013007.1:g.8016C>G
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