ClinGen Allele Registry
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Canonical Allele Identifier:
CA15605178
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.21701433T>C
GRCh37
chr9:g.21701432T>C
Linked Data - Sequence & Population
gnomAD v2:
9:21701432 T / C
gnomAD v3:
9:21701433 T / C
gnomAD v4:
chr9-21701433-T-C
Joint Max Group AF
0.7738806 (AFR)
Genomes Max Group AF
0.7738806 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7848524
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.21701433T>C , CM000671.2:g.21701433T>C
GRCh38
NC_000009.11:g.21701432T>C , CM000671.1:g.21701432T>C
GRCh37
NC_000009.10:g.21691432T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001746563.2:n.384+1484A>G
Search 100 bp 5'
Search 100 bp 3'