Canonical Allele Identifier: CA37393547
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs181406596

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214088032T>A , CM000663.2:g.214088032T>A GRCh38
NC_000001.10:g.214261375T>A , CM000663.1:g.214261375T>A GRCh37
NC_000001.9:g.212327998T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15594A>T XP_011508605.1:n.-188-15594A>T
XR_922584.1:n.119-15594A>T
XR_922584.2:n.261-15594A>T