ClinGen Allele Registry
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Canonical Allele Identifier:
CA867267446
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.79424447A>C
GRCh37
chr9:g.82039362A>C
Linked Data - NCBI & NCI
dbSNP:
2378383
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.79424447A>C , CM000671.2:g.79424447A>C
GRCh38
NC_000009.11:g.82039362A>C , CM000671.1:g.82039362A>C
GRCh37
NC_000009.10:g.81229182A>C
NCBI36
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