ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA16261779
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.34578783C>T
GRCh37
chr6:g.34546560C>T
Linked Data - Sequence & Population
gnomAD v2:
6:34546560 C / T
gnomAD v3:
6:34578783 C / T
gnomAD v4:
chr6-34578783-C-T
Joint Max Group AF
0.2694087 (AFR)
Genomes Max Group AF
0.2694087 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2814982
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.34578783C>T , CM000668.2:g.34578783C>T
GRCh38
NC_000006.11:g.34546560C>T , CM000668.1:g.34546560C>T
GRCh37
NC_000006.10:g.34654538C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'