Allele Registry

Canonical Allele Identifier: CA15092981

Gene: LINC02784 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.54527266T>C

GRCh37 chr1:g.54992939T>C

Linked Data - Sequence & Population

gnomAD v2:

1:54992939 T / C

gnomAD v3:

1:54527266 T / C

gnomAD v4:

chr1-54527266-T-C

Joint Max Group AF 0.27670395 (NFE)

Genomes Max Group AF 0.27670395 (NFE)

Linked Data - NCBI & NCI

dbSNP:

12752888

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54527266T>C , CM000663.2:g.54527266T>C	GRCh38
NC_000001.10:g.54992939T>C , CM000663.1:g.54992939T>C	GRCh37
NC_000001.9:g.54765527T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_947372.1:n.215+1266A>G
XR_947372.2:n.216+1266A>G

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