ClinGen Allele Registry
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Canonical Allele Identifier:
CA13027041
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.21747804A>G
GRCh37
chr9:g.21747803A>G
Linked Data - Sequence & Population
gnomAD v2:
9:21747803 A / G
gnomAD v3:
9:21747804 A / G
gnomAD v4:
chr9-21747804-A-G
Joint Max Group AF
0.78164321 (AFR)
Genomes Max Group AF
0.78164321 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4636294
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.21747804A>G , CM000671.2:g.21747804A>G
GRCh38
NC_000009.11:g.21747803A>G , CM000671.1:g.21747803A>G
GRCh37
NC_000009.10:g.21737803A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001746563.2:n.163+20021T>C
Search 100 bp 5'
Search 100 bp 3'