Canonical Allele Identifier: CA13489347

Gene: LINC02748

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.91223046T>C , CM000673.2:g.91223046T>C	GRCh38
NC_000011.9:g.90956214T>C , CM000673.1:g.90956214T>C	GRCh37
NC_000011.8:g.90595862T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_947881.1:n.754-4936T>C
XR_947881.3:n.779-4936T>C