Canonical Allele Identifier: CA1525089280
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs1159372896

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324121G>T , CM000667.2:g.6324121G>T GRCh38
NC_000005.9:g.6324234G>T , CM000667.1:g.6324234G>T GRCh37
NC_000005.8:g.6377234G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11405C>A