Canonical Allele Identifier: CA1623081702
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762014005

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354054T>G , CM000668.2:g.40354054T>G GRCh38
NC_000006.11:g.40321793T>G , CM000668.1:g.40321793T>G GRCh37
NC_000006.10:g.40429771T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1953A>C