Canonical Allele Identifier: CA1623081645
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762012282

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353961C>A , CM000668.2:g.40353961C>A GRCh38
NC_000006.11:g.40321700C>A , CM000668.1:g.40321700C>A GRCh37
NC_000006.10:g.40429678C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.2046G>T