Canonical Allele Identifier: CA1525089289
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs1737041725

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324139G>A , CM000667.2:g.6324139G>A GRCh38
NC_000005.9:g.6324252G>A , CM000667.1:g.6324252G>A GRCh37
NC_000005.8:g.6377252G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11423C>T