Canonical Allele Identifier: CA1623081718
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354083C= , CM000668.2:g.40354083C= GRCh38
NC_000006.11:g.40321822C= , CM000668.1:g.40321822C= GRCh37
NC_000006.10:g.40429800C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1924G=