Canonical Allele Identifier: CA1140159851
Gene: LINC01140 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.87147675T= , CM000663.2:g.87147675T= GRCh38
NC_000001.10:g.87613358T= , CM000663.1:g.87613358T= GRCh37
NC_000001.9:g.87385946T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370548.3:c.871+13957T= ENSP00000359579.1:n.871+13957T=
NR_026989.1:n.335+13957T=