Canonical Allele Identifier: CA1983856762
Gene: LINC02757 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621186A= , CM000673.2:g.76621186A= GRCh38
NC_000011.9:g.76332230A= , CM000673.1:g.76332230A= GRCh37
NC_000011.8:g.76009878A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4682T=
XR_950334.1:n.2082+5387T=
XR_001748311.1:n.2245+4682T=
XR_001748312.1:n.1515+4682T=