Canonical Allele Identifier: CA731228577
Gene: LINC02775 HGNC NCBI

Linked Data

dbSNP Id: rs1262503488
MyVariant Identifiers: chr1:g.214261021A>G (hg19) chr1:g.214087678A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087678A>G , CM000663.2:g.214087678A>G GRCh38
NC_000001.10:g.214261021A>G , CM000663.1:g.214261021A>G GRCh37
NC_000001.9:g.212327644A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15240T>C XP_011508605.1:n.-188-15240T>C
XR_922584.1:n.119-15240T>C
XR_922584.2:n.261-15240T>C
Search 100 bp 5'
Search 100 bp 3'