ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA137023731
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32891935T>C
GRCh37
chr6:g.32859712T>C
Linked Data - Sequence & Population
gnomAD v2:
6:32859712 T / C
gnomAD v3:
6:32891935 T / C
gnomAD v4:
chr6-32891935-T-C
Joint Max Group AF
0.18984306 (AFR)
Genomes Max Group AF
0.18984306 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7744666
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32891935T>C , CM000668.2:g.32891935T>C
GRCh38
NC_000006.11:g.32859712T>C , CM000668.1:g.32859712T>C
GRCh37
NC_000006.10:g.32967690T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'