Canonical Allele Identifier: CA2129250515
Gene: LINC00609 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36104812C= , CM000676.2:g.36104812C= GRCh38
NC_000014.8:g.36574018C= , CM000676.1:g.36574018C= GRCh37
NC_000014.7:g.35643769C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_073454.1:n.259+34127C=