ClinGen Allele Registry
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Canonical Allele Identifier:
CA112916443
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.1296307G>T
GRCh37
chr5:g.1296422G>T
Linked Data - Sequence & Population
gnomAD v2:
5:1296422 G / T
gnomAD v3:
5:1296307 G / T
gnomAD v4:
chr5-1296307-G-T
Joint Max Group AF
0.01120343 (AFR)
Genomes Max Group AF
0.01120343 (AFR)
Linked Data - NCBI & NCI
dbSNP:
116210138
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1296307G>T , CM000667.2:g.1296307G>T
GRCh38
NC_000005.9:g.1296422G>T , CM000667.1:g.1296422G>T
GRCh37
NC_000005.8:g.1349422G>T
NCBI36
NG_009265.1:g.3741C>A , LRG_343:g.3741C>A
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