Allele Registry

Canonical Allele Identifier: CA13888934

Gene: LINC00331 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr13:g.78807966T>C

GRCh37 chr13:g.79382101T>C

Linked Data - Sequence & Population

gnomAD v2:

13:79382101 T / C

gnomAD v3:

13:78807966 T / C

gnomAD v4:

chr13-78807966-T-C

Joint Max Group AF 0.50219483 (AFR)

Genomes Max Group AF 0.50219483 (AFR)

Linked Data - NCBI & NCI

dbSNP:

9574309

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78807966T>C , CM000675.2:g.78807966T>C	GRCh38
NC_000013.10:g.79382101T>C , CM000675.1:g.79382101T>C	GRCh37
NC_000013.9:g.78280102T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.225-15664A>G

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