Allele Registry

Canonical Allele Identifier: CA136781654

Gene: LINC00243 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr6:g.30827394A>C

GRCh37 chr6:g.30795171A>C

Linked Data - Sequence & Population

gnomAD v2:

6:30795171 A / C

gnomAD v3:

6:30827394 A / C

gnomAD v4:

chr6-30827394-A-C

Joint Max Group AF 0.03062895 (AMR)

Genomes Max Group AF 0.03062895 (AMR)

Linked Data - NCBI & NCI

dbSNP:

7772131

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30827394A>C , CM000668.2:g.30827394A>C	GRCh38
NC_000006.11:g.30795171A>C , CM000668.1:g.30795171A>C	GRCh37
NC_000006.10:g.30903150A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130726.1:n.145+3121T>G

Search 100 bp 5'

Search 100 bp 3'