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Canonical Allele Identifier:
CA28974633
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.113761198G>A
GRCh37
chr1:g.114303820G>A
Linked Data - NCBI & NCI
dbSNP:
752501335
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.113761198G>A , CM000663.2:g.113761198G>A
GRCh38
NC_000001.10:g.114303820G>A , CM000663.1:g.114303820G>A
GRCh37
NC_000001.9:g.114105343G>A
NCBI36
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