Allele Registry

Canonical Allele Identifier: CA521197909

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.12163394G>T

GRCh37 chr1:g.12223451G>T

Linked Data - Sequence & Population

gnomAD v2:

1:12223451 G / T

gnomAD v3:

1:12163394 G / T

gnomAD v4:

chr1-12163394-G-T

Linked Data - NCBI & NCI

dbSNP:

590368

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12163394G>T , CM000663.2:g.12163394G>T	GRCh38
NC_000001.10:g.12223451G>T , CM000663.1:g.12223451G>T	GRCh37
NC_000001.9:g.12146038G>T	NCBI36
NG_029791.1:g.1392G>T

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