Canonical Allele Identifier: CA1623081780
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354223C= , CM000668.2:g.40354223C= GRCh38
NC_000006.11:g.40321962C= , CM000668.1:g.40321962C= GRCh37
NC_000006.10:g.40429940C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1784G=