Canonical Allele Identifier: CA1623081722
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354089C= , CM000668.2:g.40354089C= GRCh38
NC_000006.11:g.40321828C= , CM000668.1:g.40321828C= GRCh37
NC_000006.10:g.40429806C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1918G=