Canonical Allele Identifier: CA1623081742
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1561825277

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354117C>T , CM000668.2:g.40354117C>T GRCh38
NC_000006.11:g.40321856C>T , CM000668.1:g.40321856C>T GRCh37
NC_000006.10:g.40429834C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1890G>A