ClinGen Allele Registry
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Canonical Allele Identifier:
CA16065984
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.145709377C>T
GRCh37
chr1:g.145725689G>A
Linked Data - Sequence & Population
gnomAD v2:
1:145725689 G / A
gnomAD v3:
1:145709377 C / T
gnomAD v4:
chr1-145709377-C-T
Joint Max Group AF
0.46771716 (NFE)
Genomes Max Group AF
0.46771716 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12129861
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.145709377C>T , CM000663.2:g.145709377C>T
GRCh38
NC_000001.10:g.145725689G>A , CM000663.1:g.145725689G>A
GRCh37
NC_000001.9:g.144437046G>A
NCBI36
NG_050630.1:g.3024G>A
NG_050630.2:g.3825G>A
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