Canonical Allele Identifier: CA1983856773
Gene: LINC02757 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621206T= , CM000673.2:g.76621206T= GRCh38
NC_000011.9:g.76332250T= , CM000673.1:g.76332250T= GRCh37
NC_000011.8:g.76009898T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4662A=
XR_950334.1:n.2082+5367A=
XR_001748311.1:n.2245+4662A=
XR_001748312.1:n.1515+4662A=