ClinGen Allele Registry
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Canonical Allele Identifier:
CA803700450
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.1296299C>G
GRCh37
chr5:g.1296414C>G
Linked Data - Sequence & Population
gnomAD v3:
5:1296299 C / G
gnomAD v4:
chr5-1296299-C-G
Linked Data - NCBI & NCI
dbSNP:
1457488704
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1296299C>G , CM000667.2:g.1296299C>G
GRCh38
NC_000005.9:g.1296414C>G , CM000667.1:g.1296414C>G
GRCh37
NC_000005.8:g.1349414C>G
NCBI36
NG_009265.1:g.3749G>C , LRG_343:g.3749G>C
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