Canonical Allele Identifier: CA2708089262
Gene: LINC02145 HGNC NCBI

Linked Data

dbSNP Id: rs2111393772

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6324225T>C , CM000667.2:g.6324225T>C GRCh38
NC_000005.9:g.6324338T>C , CM000667.1:g.6324338T>C GRCh37
NC_000005.8:g.6377338T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_028351.1:n.144-11509A>G