ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA891212702
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.17307027G>C
GRCh37
chr1:g.17633522G>C
Linked Data - Sequence & Population
gnomAD v3:
1:17307027 G / C
gnomAD v4:
chr1-17307027-G-C
Linked Data - NCBI & NCI
dbSNP:
2501796
2100212525
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.17307027G>C , CM000663.2:g.17307027G>C
GRCh38
NC_000001.10:g.17633522G>C , CM000663.1:g.17633522G>C
GRCh37
NC_000001.9:g.17506109G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'