Allele Registry

Canonical Allele Identifier: CA761189265

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.177044867T>G

GRCh37 chr2:g.177909595T>G

Linked Data - Sequence & Population

gnomAD v3:

2:177044867 T / G

gnomAD v4:

chr2-177044867-T-G

Linked Data - NCBI & NCI

dbSNP:

1529093

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177044867T>G , CM000664.2:g.177044867T>G	GRCh38
NC_000002.11:g.177909595T>G , CM000664.1:g.177909595T>G	GRCh37
NC_000002.10:g.177617841T>G	NCBI36

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