Canonical Allele Identifier: CA1623081732
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1466965954

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354107A>T , CM000668.2:g.40354107A>T GRCh38
NC_000006.11:g.40321846A>T , CM000668.1:g.40321846A>T GRCh37
NC_000006.10:g.40429824A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1900T>A