ClinGen Allele Registry
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Canonical Allele Identifier:
CA195699255
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.90124949C>T
GRCh37
chr9:g.92887231C>T
Linked Data - Sequence & Population
gnomAD v2:
9:92887231 C / T
gnomAD v3:
9:90124949 C / T
gnomAD v4:
chr9-90124949-C-T
Joint Max Group AF
0.20255445 (AFR)
Genomes Max Group AF
0.20255445 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2081670
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.90124949C>T , CM000671.2:g.90124949C>T
GRCh38
NC_000009.11:g.92887231C>T , CM000671.1:g.92887231C>T
GRCh37
NC_000009.10:g.91927051C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'