Canonical Allele Identifier: CA1983856759
Gene: LINC02757 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621175T= , CM000673.2:g.76621175T= GRCh38
NC_000011.9:g.76332219T= , CM000673.1:g.76332219T= GRCh37
NC_000011.8:g.76009867T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4693A=
XR_950334.1:n.2082+5398A=
XR_001748311.1:n.2245+4693A=
XR_001748312.1:n.1515+4693A=