Canonical Allele Identifier: CA2780866021

Gene: MIR2052HG LINC03071

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74615273A>C , CM000670.2:g.74615273A>C	GRCh38
NC_000008.10:g.75527508A>C , CM000670.1:g.75527508A>C	GRCh37
NC_000008.9:g.75690063A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033830.1:n.131+2333A>C (MIR2052HG)
XR_929054.1:n.345+1487T>G (LINC03071)
XR_929055.1:n.165-2707T>G (LINC03071)
XR_929056.1:n.345+1487T>G (LINC03071)
XR_929057.1:n.222+1487T>G (LINC03071)
XR_001745957.1:n.628+1487T>G (LINC03071)
XR_001745958.1:n.448-2707T>G (LINC03071)
XR_001745960.1:n.222+1487T>G (LINC03071)
XR_002956714.1:n.628+1487T>G (LINC03071)