ClinGen Allele Registry
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Canonical Allele Identifier:
CA803700510
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.1296375C>T
GRCh37
chr5:g.1296490C>T
Linked Data - Sequence & Population
gnomAD v3:
5:1296375 C / T
gnomAD v4:
chr5-1296375-C-T
Joint Max Group AF
0.00050273 (AMR)
Genomes Max Group AF
0.00050273 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1197804910
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1296375C>T , CM000667.2:g.1296375C>T
GRCh38
NC_000005.9:g.1296490C>T , CM000667.1:g.1296490C>T
GRCh37
NC_000005.8:g.1349490C>T
NCBI36
NG_009265.1:g.3673G>A , LRG_343:g.3673G>A
Search 100 bp 5'
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