Canonical Allele Identifier: CA12889921

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>C , CM000670.2:g.10477271T>C	GRCh38
NC_000008.10:g.10334781T>C , CM000670.1:g.10334781T>C	GRCh37
NC_000008.9:g.10372191T>C	NCBI36

Transcript Alleles

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