ClinGen Allele Registry
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Canonical Allele Identifier:
CA21833164
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.45329017A>G
GRCh37
chr1:g.45794689A>G
Linked Data - NCBI & NCI
dbSNP:
368743158
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.45329017A>G , CM000663.2:g.45329017A>G
GRCh38
NC_000001.10:g.45794689A>G , CM000663.1:g.45794689A>G
GRCh37
NC_000001.9:g.45567276A>G
NCBI36
NG_008189.1:g.16454T>C , LRG_220:g.16454T>C
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