Canonical Allele Identifier: CA1983856763

Gene: LINC02757

Linked Data

• dbSNP Id: rs1952222965

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76621186A>T , CM000673.2:g.76621186A>T	GRCh38
NC_000011.9:g.76332230A>T , CM000673.1:g.76332230A>T	GRCh37
NC_000011.8:g.76009878A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247265.2:n.2147+4682T>A
XR_950334.1:n.2082+5387T>A
XR_001748311.1:n.2245+4682T>A
XR_001748312.1:n.1515+4682T>A