Canonical Allele Identifier: CA1983856775
Gene: LINC02757 HGNC NCBI

Linked Data

dbSNP Id: rs1952223135

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76621207A>G , CM000673.2:g.76621207A>G GRCh38
NC_000011.9:g.76332251A>G , CM000673.1:g.76332251A>G GRCh37
NC_000011.8:g.76009899A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247265.2:n.2147+4661T>C
XR_950334.1:n.2082+5366T>C
XR_001748311.1:n.2245+4661T>C
XR_001748312.1:n.1515+4661T>C