ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12140166
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.18483542C>T
GRCh37
chr5:g.18483651C>T
Linked Data - Sequence & Population
gnomAD v2:
5:18483651 C / T
gnomAD v3:
5:18483542 C / T
gnomAD v4:
chr5-18483542-C-T
Joint Max Group AF
0.95023408 (SAS)
Genomes Max Group AF
0.95023408 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4866334
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.18483542C>T , CM000667.2:g.18483542C>T
GRCh38
NC_000005.9:g.18483651C>T , CM000667.1:g.18483651C>T
GRCh37
NC_000005.8:g.18519408C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'