ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA573387860
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.26143114T>C
GRCh37
chr7:g.26182734T>C
Linked Data - Sequence & Population
gnomAD v2:
7:26182734 T / C
gnomAD v3:
7:26143114 T / C
gnomAD v4:
chr7-26143114-T-C
Joint Max Group AF
0.00021497 (AMR)
Genomes Max Group AF
0.00021497 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1272318687
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.26143114T>C , CM000669.2:g.26143114T>C
GRCh38
NC_000007.13:g.26182734T>C , CM000669.1:g.26182734T>C
GRCh37
NC_000007.12:g.26149259T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'