Canonical Allele Identifier: CA1983856758
Gene: LINC02757 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621172C= , CM000673.2:g.76621172C= GRCh38
NC_000011.9:g.76332216C= , CM000673.1:g.76332216C= GRCh37
NC_000011.8:g.76009864C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4696G=
XR_950334.1:n.2082+5401G=
XR_001748311.1:n.2245+4696G=
XR_001748312.1:n.1515+4696G=