Allele Registry

Canonical Allele Identifier: CA136829026

Gene: LINC02571 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr6:g.31295974T>C

GRCh37 chr6:g.31263751T>C

Linked Data - Sequence & Population

gnomAD v2:

6:31263751 T / C

gnomAD v3:

6:31295974 T / C

gnomAD v4:

chr6-31295974-T-C

Joint Max Group AF 0.29555779 (MID)

Genomes Max Group AF 0.29042116 (SAS)

Linked Data - NCBI & NCI

dbSNP:

2894207

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31295974T>C , CM000668.2:g.31295974T>C	GRCh38
NC_000006.11:g.31263751T>C , CM000668.1:g.31263751T>C	GRCh37
NC_000006.10:g.31371730T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_149115.1:n.167-961A>G

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