Canonical Allele Identifier: CA1635715675
Gene: LINC02549 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.68275038T= , CM000668.2:g.68275038T= GRCh38
NC_000006.11:g.68984930T= , CM000668.1:g.68984930T= GRCh37
NC_000006.10:g.69041651T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125854.1:n.238-8423A=