Canonical Allele Identifier: CA2559014920
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353987G>A , CM000668.2:g.40353987G>A GRCh38
NC_000006.11:g.40321726G>A , CM000668.1:g.40321726G>A GRCh37
NC_000006.10:g.40429704G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.2020C>T