ClinGen Allele Registry
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Canonical Allele Identifier:
CA805081867
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.1447745C>G
GRCh37
chr5:g.1447860C>G
Linked Data - NCBI & NCI
dbSNP:
2652510
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1447745C>G , CM000667.2:g.1447745C>G
GRCh38
NC_000005.9:g.1447860C>G , CM000667.1:g.1447860C>G
GRCh37
NC_000005.8:g.1500860C>G
NCBI36
NG_015885.1:g.2684G>C
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