ClinGen Allele Registry
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Canonical Allele Identifier:
CA11664958
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.154602694A>T
GRCh37
chr4:g.155523846A>T
Linked Data - Sequence & Population
gnomAD v2:
4:155523846 A / T
gnomAD v3:
4:154602694 A / T
gnomAD v4:
chr4-154602694-A-T
Joint Max Group AF
0.78203452 (EAS)
Genomes Max Group AF
0.78203452 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1118823
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.154602694A>T , CM000666.2:g.154602694A>T
GRCh38
NC_000004.11:g.155523846A>T , CM000666.1:g.155523846A>T
GRCh37
NC_000004.10:g.155743296A>T
NCBI36
NG_008834.1:g.15057T>A
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