Canonical Allele Identifier: CA15753317
Gene: LINC02398 HGNC NCBI

Linked Data

dbSNP Id: rs2728554

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20062248T>G , CM000674.2:g.20062248T>G GRCh38
NC_000012.11:g.20215182T>G , CM000674.1:g.20215182T>G GRCh37
NC_000012.10:g.20106449T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040098.1:n.410-36504T>G