ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA837112708
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.26143150C>T
GRCh37
chr7:g.26182770C>T
Linked Data - Sequence & Population
gnomAD v3:
7:26143150 C / T
gnomAD v4:
chr7-26143150-C-T
Linked Data - NCBI & NCI
dbSNP:
1273972193
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.26143150C>T , CM000669.2:g.26143150C>T
GRCh38
NC_000007.13:g.26182770C>T , CM000669.1:g.26182770C>T
GRCh37
NC_000007.12:g.26149295C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'