Canonical Allele Identifier: CA1623081769
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354195G= , CM000668.2:g.40354195G= GRCh38
NC_000006.11:g.40321934G= , CM000668.1:g.40321934G= GRCh37
NC_000006.10:g.40429912G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1812C=