Canonical Allele Identifier: CA48805968

Gene: LINC01122

Linked Data

• dbSNP Id: rs1050714511
• MyVariant Identifiers: chr2:g.59036855T>A (hg19) ; chr2:g.58809720T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.58809720T>A , CM000664.2:g.58809720T>A	GRCh38
NC_000002.11:g.59036855T>A , CM000664.1:g.59036855T>A	GRCh37
NC_000002.10:g.58890359T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033873.1:n.248-40710T>A