ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA16244762
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.147845951T>C
GRCh37
chr5:g.147225514T>C
Linked Data - Sequence & Population
gnomAD v2:
5:147225514 T / C
gnomAD v3:
5:147845951 T / C
gnomAD v4:
chr5-147845951-T-C
Joint Max Group AF
0.29561489 (EAS)
Genomes Max Group AF
0.29561489 (EAS)
Linked Data - NCBI & NCI
dbSNP:
891992
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.147845951T>C , CM000667.2:g.147845951T>C
GRCh38
NC_000005.9:g.147225514T>C , CM000667.1:g.147225514T>C
GRCh37
NC_000005.8:g.147205707T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'