Canonical Allele Identifier: CA1796642566
Gene: LINC01607 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79779234A= , CM000670.2:g.79779234A= GRCh38
NC_000008.10:g.80691469A= , CM000670.1:g.80691469A= GRCh37
NC_000008.9:g.80854024A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110954.1:n.437-7612T=
NR_125410.1:n.139-774A=