ClinGen Allele Registry
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Canonical Allele Identifier:
CA837112699
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.26143139T>A
GRCh37
chr7:g.26182759T>A
Linked Data - Sequence & Population
gnomAD v3:
7:26143139 T / A
gnomAD v4:
chr7-26143139-T-A
Joint Max Group AF
0.00001171 (NFE)
Genomes Max Group AF
0.00001171 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1208838757
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.26143139T>A , CM000669.2:g.26143139T>A
GRCh38
NC_000007.13:g.26182759T>A , CM000669.1:g.26182759T>A
GRCh37
NC_000007.12:g.26149284T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'