Canonical Allele Identifier: CA172331271

Gene: LINC03022

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.10477271T>G , CM000670.2:g.10477271T>G	GRCh38
NC_000008.10:g.10334781T>G , CM000670.1:g.10334781T>G	GRCh37
NC_000008.9:g.10372191T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120604.1:n.216T>G