Canonical Allele Identifier: CA1623081771
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1666963916

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354200G>C , CM000668.2:g.40354200G>C GRCh38
NC_000006.11:g.40321939G>C , CM000668.1:g.40321939G>C GRCh37
NC_000006.10:g.40429917G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1807C>G