Canonical Allele Identifier: CA2581062075
Gene: LINC02757 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621166T>A , CM000673.2:g.76621166T>A GRCh38
NC_000011.9:g.76332210T>A , CM000673.1:g.76332210T>A GRCh37
NC_000011.8:g.76009858T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4702A>T
XR_950334.1:n.2082+5407A>T
XR_001748311.1:n.2245+4702A>T
XR_001748312.1:n.1515+4702A>T