Canonical Allele Identifier: CA855256143

Gene: MIR2052HG LINC03071

Linked Data

• dbSNP Id: rs1411902565
• MyVariant Identifiers: chr8:g.75527536T>A (hg19) ; chr8:g.74615301T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74615301T>A , CM000670.2:g.74615301T>A	GRCh38
NC_000008.10:g.75527536T>A , CM000670.1:g.75527536T>A	GRCh37
NC_000008.9:g.75690091T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_033830.1:n.131+2361T>A (MIR2052HG)
XR_929054.1:n.345+1459A>T (LINC03071)
XR_929055.1:n.165-2735A>T (LINC03071)
XR_929056.1:n.345+1459A>T (LINC03071)
XR_929057.1:n.222+1459A>T (LINC03071)
XR_001745957.1:n.628+1459A>T (LINC03071)
XR_001745958.1:n.448-2735A>T (LINC03071)
XR_001745960.1:n.222+1459A>T (LINC03071)
XR_002956714.1:n.628+1459A>T (LINC03071)