ClinGen Allele Registry
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Canonical Allele Identifier:
CA598527383
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.35232539T>C
GRCh37
chr11:g.35254086T>C
Linked Data - Sequence & Population
gnomAD v2:
11:35254086 T / C
gnomAD v3:
11:35232539 T / C
gnomAD v4:
chr11-35232539-T-C
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4755392
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.35232539T>C , CM000673.2:g.35232539T>C
GRCh38
NC_000011.9:g.35254086T>C , CM000673.1:g.35254086T>C
GRCh37
NC_000011.8:g.35210662T>C
NCBI36
NG_008937.1:g.98670T>C
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