ClinGen Allele Registry
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Canonical Allele Identifier:
CA890209317
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.161502368A>T
GRCh37
chr1:g.161472158A>T
Linked Data - NCBI & NCI
dbSNP:
10800309
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.161502368A>T , CM000663.2:g.161502368A>T
GRCh38
NC_000001.10:g.161472158A>T , CM000663.1:g.161472158A>T
GRCh37
NC_000001.9:g.159738782A>T
NCBI36
NG_012066.1:g.1954A>T
NG_012066.2:g.1954A>T
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