ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13944296
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.80120798T>C
GRCh37
chr14:g.80587141T>C
Linked Data - Sequence & Population
gnomAD v2:
14:80587141 T / C
gnomAD v3:
14:80120798 T / C
gnomAD v4:
chr14-80120798-T-C
Joint Max Group AF
0.73237736 (AFR)
Genomes Max Group AF
0.73237736 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10220309
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.80120798T>C , CM000676.2:g.80120798T>C
GRCh38
NC_000014.8:g.80587141T>C , CM000676.1:g.80587141T>C
GRCh37
NC_000014.7:g.79656894T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'