ClinGen Allele Registry
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Canonical Allele Identifier:
CA12642378
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr7:g.150990599C>T
GRCh37
chr7:g.150687687C>T
Linked Data - Sequence & Population
gnomAD v2:
7:150687687 C / T
gnomAD v3:
7:150990599 C / T
gnomAD v4:
chr7-150990599-C-T
Joint Max Group AF
0.40802652 (EAS)
Genomes Max Group AF
0.40802652 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11771443
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.150990599C>T , CM000669.2:g.150990599C>T
GRCh38
NC_000007.13:g.150687687C>T , CM000669.1:g.150687687C>T
GRCh37
NC_000007.12:g.150318620C>T
NCBI36
NG_011992.1:g.4541C>T
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