Canonical Allele Identifier: CA1623081674
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354004G= , CM000668.2:g.40354004G= GRCh38
NC_000006.11:g.40321743G= , CM000668.1:g.40321743G= GRCh37
NC_000006.10:g.40429721G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.2003C=