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Canonical Allele Identifier:
CA13041617
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.136965812T>C
GRCh37
chr9:g.139860264T>C
Linked Data - Sequence & Population
gnomAD v2:
9:139860264 T / C
gnomAD v3:
9:136965812 T / C
gnomAD v4:
chr9-136965812-T-C
Joint Max Group AF
0.51243448 (AMR)
Genomes Max Group AF
0.51243448 (AMR)
Linked Data - NCBI & NCI
dbSNP:
11145951
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.136965812T>C , CM000671.2:g.136965812T>C
GRCh38
NC_000009.11:g.139860264T>C , CM000671.1:g.139860264T>C
GRCh37
NC_000009.10:g.138980085T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'