Canonical Allele Identifier: CA1983856777
Gene: LINC02757 HGNC NCBI

Linked Data

dbSNP Id: rs1952223145

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621210T>A , CM000673.2:g.76621210T>A GRCh38
NC_000011.9:g.76332254T>A , CM000673.1:g.76332254T>A GRCh37
NC_000011.8:g.76009902T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4658A>T
XR_950334.1:n.2082+5363A>T
XR_001748311.1:n.2245+4658A>T
XR_001748312.1:n.1515+4658A>T