Canonical Allele Identifier: CA1623081689
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762013588

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354026T>C , CM000668.2:g.40354026T>C GRCh38
NC_000006.11:g.40321765T>C , CM000668.1:g.40321765T>C GRCh37
NC_000006.10:g.40429743T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1981A>G