Canonical Allele Identifier: CA14052468
Gene: LINC00609 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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