Canonical Allele Identifier: CA1140179915
Gene: LINC01363 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.167187263T= , CM000663.2:g.167187263T= GRCh38
NC_000001.10:g.167156500T= , CM000663.1:g.167156500T= GRCh37
NC_000001.9:g.165423124T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110811.1:n.249-5070A=