Allele Registry

Canonical Allele Identifier: CA60587195

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr2:g.170684313A>T

GRCh37 chr2:g.171540823A>T

Linked Data - Sequence & Population

gnomAD v2:

2:171540823 A / T

gnomAD v3:

2:170684313 A / T

gnomAD v4:

chr2-170684313-A-T

Linked Data - NCBI & NCI

dbSNP:

2080401

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.170684313A>T , CM000664.2:g.170684313A>T	GRCh38
NC_000002.11:g.171540823A>T , CM000664.1:g.171540823A>T	GRCh37
NC_000002.10:g.171249069A>T	NCBI36

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