ClinGen Allele Registry
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Canonical Allele Identifier:
CA11915807
Gene:
Linked Data
ClinVar Variation Id:
375479
ClinVar RCV Id:
RCV000498732
RCV001787099
dbSNP Id:
rs2735940
gnomAD v2:
5-1296486-A-G
gnomAD v3:
5-1296371-A-G
gnomAD v4:
5-1296371-A-G
MyVariant Identifiers:
chr5:g.1296486A>G (hg19)
chr5:g.1296371A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1296371A>G , CM000667.2:g.1296371A>G
GRCh38
NC_000005.9:g.1296486A>G , CM000667.1:g.1296486A>G
GRCh37
NC_000005.8:g.1349486A>G
NCBI36
NG_009265.1:g.3677T>C , LRG_343:g.3677T>C
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