ClinGen Allele Registry
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Canonical Allele Identifier:
CA737442901
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.59928177A>G
GRCh37
chr1:g.60393849A>G
Linked Data - NCBI & NCI
dbSNP:
11572182
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.59928177A>G , CM000663.2:g.59928177A>G
GRCh38
NC_000001.10:g.60393849A>G , CM000663.1:g.60393849A>G
GRCh37
NC_000001.9:g.60166437A>G
NCBI36
NG_007931.1:g.3575T>C
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