ClinGen Allele Registry
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Canonical Allele Identifier:
CA11793089
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.154560211T>C
GRCh37
chr4:g.155481363T>C
Linked Data - Sequence & Population
gnomAD v2:
4:155481363 T / C
gnomAD v3:
4:154560211 T / C
gnomAD v4:
chr4-154560211-T-C
Joint Max Group AF
0.53129039 (EAS)
Genomes Max Group AF
0.53129039 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1025154
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.154560211T>C , CM000666.2:g.154560211T>C
GRCh38
NC_000004.11:g.155481363T>C , CM000666.1:g.155481363T>C
GRCh37
NC_000004.10:g.155700813T>C
NCBI36
NG_008833.1:g.2232T>C , LRG_558:g.2232T>C
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