Canonical Allele Identifier: CA110561426
Gene: LINC02275 HGNC NCBI

Linked Data

dbSNP Id: rs11723530

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.169959732G>A , CM000666.2:g.169959732G>A GRCh38
NC_000004.11:g.170880883G>A , CM000666.1:g.170880883G>A GRCh37
NC_000004.10:g.171117458G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_037878.1:n.87+16084C>T