ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11180365
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.19745816T>C
GRCh37
chr2:g.19945577T>C
Linked Data - Sequence & Population
gnomAD v2:
2:19945577 T / C
gnomAD v3:
2:19745816 T / C
gnomAD v4:
chr2-19745816-T-C
Joint Max Group AF
0.94002629 (NFE)
Genomes Max Group AF
0.94002629 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2123536
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.19745816T>C , CM000664.2:g.19745816T>C
GRCh38
NC_000002.11:g.19945577T>C , CM000664.1:g.19945577T>C
GRCh37
NC_000002.10:g.19809058T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'