Allele Registry

Canonical Allele Identifier: CA590283360

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.114806918T>C

GRCh37 chr9:g.117569198T>C

Linked Data - Sequence & Population

gnomAD v2:

9:117569198 T / C

gnomAD v3:

9:114806918 T / C

gnomAD v4:

chr9-114806918-T-C

Linked Data - NCBI & NCI

dbSNP:

1356503474

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114806918T>C , CM000671.2:g.114806918T>C	GRCh38
NC_000009.11:g.117569198T>C , CM000671.1:g.117569198T>C	GRCh37
NC_000009.10:g.116609019T>C	NCBI36
NG_011488.2:g.4211A>G

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