Allele Registry

Canonical Allele Identifier: CA11122031

Gene: LINC01965 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr2:g.103956547C>T

GRCh37 chr2:g.104573005C>T

Linked Data - Sequence & Population

gnomAD v2:

2:104573005 C / T

gnomAD v3:

2:103956547 C / T

gnomAD v4:

chr2-103956547-C-T

Joint Max Group AF 0.23037771 (EAS)

Genomes Max Group AF 0.23037771 (EAS)

Linked Data - NCBI & NCI

dbSNP:

2119507

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103956547C>T , CM000664.2:g.103956547C>T	GRCh38
NC_000002.11:g.104573005C>T , CM000664.1:g.104573005C>T	GRCh37
NC_000002.10:g.103939437C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739621.1:n.178+82102C>T
XR_001739623.1:n.178+82102C>T

Search 100 bp 5'

Search 100 bp 3'