ClinGen Allele Registry
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Canonical Allele Identifier:
CA11867786
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.156077389T>C
GRCh37
chr4:g.156998541T>C
Linked Data - Sequence & Population
gnomAD v2:
4:156998541 T / C
gnomAD v3:
4:156077389 T / C
gnomAD v4:
chr4-156077389-T-C
Joint Max Group AF
0.87651971 (NFE)
Genomes Max Group AF
0.87651971 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4234898
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.156077389T>C , CM000666.2:g.156077389T>C
GRCh38
NC_000004.11:g.156998541T>C , CM000666.1:g.156998541T>C
GRCh37
NC_000004.10:g.157217991T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'