Canonical Allele Identifier: CA1514142878
Gene: LINC02268 HGNC NCBI

Linked Data

dbSNP Id: rs1039704993

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106414A>G , CM000666.2:g.174106414A>G GRCh38
NC_000004.11:g.175027565A>G , CM000666.1:g.175027565A>G GRCh37
NC_000004.10:g.175264140A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125896.1:n.276-8585T>C
XR_939484.1:n.877+18775A>G
XR_939485.1:n.877+18775A>G