Canonical Allele Identifier: CA1623081770
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354200G= , CM000668.2:g.40354200G= GRCh38
NC_000006.11:g.40321939G= , CM000668.1:g.40321939G= GRCh37
NC_000006.10:g.40429917G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1807C=