Canonical Allele Identifier: CA1140431673
Gene: LINC02784 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54527266T= , CM000663.2:g.54527266T= GRCh38
NC_000001.10:g.54992939T= , CM000663.1:g.54992939T= GRCh37
NC_000001.9:g.54765527T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947372.1:n.215+1266A=
XR_947372.2:n.216+1266A=