Canonical Allele Identifier: CA2536339662
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354271C>T , CM000668.2:g.40354271C>T GRCh38
NC_000006.11:g.40322010C>T , CM000668.1:g.40322010C>T GRCh37
NC_000006.10:g.40429988C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1736G>A