Allele Registry

Canonical Allele Identifier: CA14060150

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr14:g.35405648T>C

GRCh37 chr14:g.35874854T>C

Linked Data - Sequence & Population

gnomAD v2:

14:35874854 T / C

gnomAD v3:

14:35405648 T / C

gnomAD v4:

chr14-35405648-T-C

Joint Max Group AF 0.28616192 (NFE)

Genomes Max Group AF 0.28616192 (NFE)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV001517841

ClinVar Variation:

1167990

dbSNP:

3138053

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35405648T>C , CM000676.2:g.35405648T>C	GRCh38
NC_000014.8:g.35874854T>C , CM000676.1:g.35874854T>C	GRCh37
NC_000014.7:g.34944605T>C	NCBI36
NG_007571.1:g.4091A>G , LRG_89:g.4091A>G

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