ClinGen Allele Registry
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Canonical Allele Identifier:
CA129189653
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.150843825T>C
GRCh37
chr5:g.150223387T>C
Linked Data - Sequence & Population
gnomAD v2:
5:150223387 T / C
gnomAD v3:
5:150843825 T / C
gnomAD v4:
chr5-150843825-T-C
Joint Max Group AF
0.43652483 (AFR)
Genomes Max Group AF
0.43652483 (AFR)
Linked Data - NCBI & NCI
dbSNP:
13361189
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.150843825T>C , CM000667.2:g.150843825T>C
GRCh38
NC_000005.9:g.150223387T>C , CM000667.1:g.150223387T>C
GRCh37
NC_000005.8:g.150203580T>C
NCBI36
NG_027809.1:g.2303T>C
NG_027809.2:g.2303T>C
Search 100 bp 5'
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