Allele Registry

Canonical Allele Identifier: CA221324977

Gene: LINC01499 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr11:g.41831114T>C

GRCh37 chr11:g.41852664T>C

Linked Data - Sequence & Population

gnomAD v2:

11:41852664 T / C

gnomAD v3:

11:41831114 T / C

gnomAD v4:

chr11-41831114-T-C

Joint Max Group AF 0.27189986 (SAS)

Genomes Max Group AF 0.27189986 (SAS)

Linked Data - NCBI & NCI

dbSNP:

1484948

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.41831114T>C , CM000673.2:g.41831114T>C	GRCh38
NC_000011.9:g.41852664T>C , CM000673.1:g.41852664T>C	GRCh37
NC_000011.8:g.41809240T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120584.1:n.370-4057T>C

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