ClinGen Allele Registry
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Canonical Allele Identifier:
CA735044026
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.32290838T>A
GRCh37
chr1:g.32756439T>A
Linked Data - NCBI & NCI
dbSNP:
1741981
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.32290838T>A , CM000663.2:g.32290838T>A
GRCh38
NC_000001.10:g.32756439T>A , CM000663.1:g.32756439T>A
GRCh37
NC_000001.9:g.32529026T>A
NCBI36
NG_047018.1:g.3732T>A
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