Allele Registry

Canonical Allele Identifier: CA590283364

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.114806949A>G

GRCh37 chr9:g.117569229A>G

Linked Data - Sequence & Population

gnomAD v2:

9:117569229 A / G

gnomAD v3:

9:114806949 A / G

gnomAD v4:

chr9-114806949-A-G

Linked Data - NCBI & NCI

dbSNP:

1467958231

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114806949A>G , CM000671.2:g.114806949A>G	GRCh38
NC_000009.11:g.117569229A>G , CM000671.1:g.117569229A>G	GRCh37
NC_000009.10:g.116609050A>G	NCBI36
NG_011488.2:g.4180T>C

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