Canonical Allele Identifier: CA1623081704
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762014025

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354056G>A , CM000668.2:g.40354056G>A GRCh38
NC_000006.11:g.40321795G>A , CM000668.1:g.40321795G>A GRCh37
NC_000006.10:g.40429773G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1951C>T