Allele Registry

Canonical Allele Identifier: CA36875466

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.212700089C>G

GRCh37 chr1:g.212873431C>G

Linked Data - Sequence & Population

gnomAD v3:

1:212700089 C / G

gnomAD v4:

chr1-212700089-C-G

Linked Data - NCBI & NCI

dbSNP:

2221593

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.212700089C>G , CM000663.2:g.212700089C>G	GRCh38
NC_000001.10:g.212873431C>G , CM000663.1:g.212873431C>G	GRCh37
NC_000001.9:g.210940054C>G	NCBI36

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