Canonical Allele Identifier: CA1623081639
Gene: LINC00951 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353948A= , CM000668.2:g.40353948A= GRCh38
NC_000006.11:g.40321687A= , CM000668.1:g.40321687A= GRCh37
NC_000006.10:g.40429665A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.2059T=