ClinGen Allele Registry
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Canonical Allele Identifier:
CA14776192
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.46007096T>A
GRCh37
chr20:g.44635735T>A
Linked Data - Sequence & Population
gnomAD v2:
20:44635735 T / A
gnomAD v3:
20:46007096 T / A
gnomAD v4:
chr20-46007096-T-A
Joint Max Group AF
0.22194626 (SAS)
Genomes Max Group AF
0.22194626 (SAS)
Linked Data - NCBI & NCI
dbSNP:
3918241
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.46007096T>A , CM000682.2:g.46007096T>A
GRCh38
NC_000020.10:g.44635735T>A , CM000682.1:g.44635735T>A
GRCh37
NC_000020.9:g.44069142T>A
NCBI36
NG_011468.1:g.3189T>A
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