Canonical Allele Identifier: CA1623081658
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1581657068

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353982G>A , CM000668.2:g.40353982G>A GRCh38
NC_000006.11:g.40321721G>A , CM000668.1:g.40321721G>A GRCh37
NC_000006.10:g.40429699G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.2025C>T