ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10973328
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.183021513C>T
GRCh37
chr1:g.182990648C>T
Linked Data - Sequence & Population
gnomAD v2:
1:182990648 C / T
gnomAD v3:
1:183021513 C / T
gnomAD v4:
chr1-183021513-C-T
Joint Max Group AF
0.19581342 (AMR)
Genomes Max Group AF
0.19581342 (AMR)
Linked Data - NCBI & NCI
dbSNP:
10911193
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.183021513C>T , CM000663.2:g.183021513C>T
GRCh38
NC_000001.10:g.182990648C>T , CM000663.1:g.182990648C>T
GRCh37
NC_000001.9:g.181257271C>T
NCBI36
NG_011463.1:g.3054C>T
Search 100 bp 5'
Search 100 bp 3'