Canonical Allele Identifier: CA1623081700
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1581657106

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354052T>A , CM000668.2:g.40354052T>A GRCh38
NC_000006.11:g.40321791T>A , CM000668.1:g.40321791T>A GRCh37
NC_000006.10:g.40429769T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1955A>T