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Canonical Allele Identifier:
CA12337780
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.149113975T>C
GRCh37
chr6:g.149435111T>C
Linked Data - Sequence & Population
gnomAD v2:
6:149435111 T / C
gnomAD v3:
6:149113975 T / C
gnomAD v4:
chr6-149113975-T-C
Joint Max Group AF
0.5032784 (AFR)
Genomes Max Group AF
0.5032784 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7772697
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.149113975T>C , CM000668.2:g.149113975T>C
GRCh38
NC_000006.11:g.149435111T>C , CM000668.1:g.149435111T>C
GRCh37
NC_000006.10:g.149476804T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'