Canonical Allele Identifier: CA1623081690
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354028T= , CM000668.2:g.40354028T= GRCh38
NC_000006.11:g.40321767T= , CM000668.1:g.40321767T= GRCh37
NC_000006.10:g.40429745T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1979A=