Canonical Allele Identifier: CA2770756665
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354209T>C , CM000668.2:g.40354209T>C GRCh38
NC_000006.11:g.40321948T>C , CM000668.1:g.40321948T>C GRCh37
NC_000006.10:g.40429926T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1798A>G