ClinGen Allele Registry
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Canonical Allele Identifier:
CA11702695
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.141636126T>A
GRCh37
chr4:g.142557279T>A
Linked Data - Sequence & Population
gnomAD v2:
4:142557279 T / A
gnomAD v3:
4:141636126 T / A
gnomAD v4:
chr4-141636126-T-A
Joint Max Group AF
0.18040812 (SAS)
Genomes Max Group AF
0.18040812 (SAS)
Linked Data - NCBI & NCI
dbSNP:
3806798
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.141636126T>A , CM000666.2:g.141636126T>A
GRCh38
NC_000004.11:g.142557279T>A , CM000666.1:g.142557279T>A
GRCh37
NC_000004.10:g.142776729T>A
NCBI36
NG_029605.1:g.4531T>A
NG_029605.2:g.4531T>A
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