Canonical Allele Identifier: CA1623081779
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354221G= , CM000668.2:g.40354221G= GRCh38
NC_000006.11:g.40321960G= , CM000668.1:g.40321960G= GRCh37
NC_000006.10:g.40429938G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1786C=