ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA58479190
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.150869278G>C
GRCh37
chr2:g.151725792G>C
Linked Data - Sequence & Population
gnomAD v2:
2:151725792 G / C
gnomAD v3:
2:150869278 G / C
gnomAD v4:
chr2-150869278-G-C
Joint Max Group AF
0.00009542 (AFR)
Genomes Max Group AF
0.00009542 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10195263
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.150869278G>C , CM000664.2:g.150869278G>C
GRCh38
NC_000002.11:g.151725792G>C , CM000664.1:g.151725792G>C
GRCh37
NC_000002.10:g.151434038G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'