Canonical Allele Identifier: CA1623081752
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354160A= , CM000668.2:g.40354160A= GRCh38
NC_000006.11:g.40321899A= , CM000668.1:g.40321899A= GRCh37
NC_000006.10:g.40429877A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1847T=