Canonical Allele Identifier: CA224770967

Gene: LINC02757

Linked Data

• dbSNP Id: rs116505259
• MyVariant Identifiers: chr11:g.76621185A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76621185A>G , CM000673.2:g.76621185A>G	GRCh38
NC_000011.9:g.76332229A>G , CM000673.1:g.76332229A>G	GRCh37
NC_000011.8:g.76009877A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247265.2:n.2147+4683T>C
XR_950334.1:n.2082+5388T>C
XR_001748311.1:n.2245+4683T>C
XR_001748312.1:n.1515+4683T>C