Canonical Allele Identifier: CA1924922250
Gene: LINC01519 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85193571A= , CM000672.2:g.85193571A= GRCh38
NC_000010.10:g.86953327A= , CM000672.1:g.86953327A= GRCh37
NC_000010.9:g.86943307A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120667.1:n.1897T=
NR_120668.1:n.1050T=