Canonical Allele Identifier: CA1983856768
Gene: LINC02757 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621199G= , CM000673.2:g.76621199G= GRCh38
NC_000011.9:g.76332243G= , CM000673.1:g.76332243G= GRCh37
NC_000011.8:g.76009891G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4669C=
XR_950334.1:n.2082+5374C=
XR_001748311.1:n.2245+4669C=
XR_001748312.1:n.1515+4669C=