Canonical Allele Identifier: CA2717491788

Gene: MIR2052HG LINC03071

Linked Data

• dbSNP Id: rs2128731878

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74615386T>C , CM000670.2:g.74615386T>C	GRCh38
NC_000008.10:g.75527621T>C , CM000670.1:g.75527621T>C	GRCh37
NC_000008.9:g.75690176T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033830.1:n.131+2446T>C (MIR2052HG)
XR_929054.1:n.345+1374A>G (LINC03071)
XR_929055.1:n.165-2820A>G (LINC03071)
XR_929056.1:n.345+1374A>G (LINC03071)
XR_929057.1:n.222+1374A>G (LINC03071)
XR_001745957.1:n.628+1374A>G (LINC03071)
XR_001745958.1:n.448-2820A>G (LINC03071)
XR_001745960.1:n.222+1374A>G (LINC03071)
XR_002956714.1:n.628+1374A>G (LINC03071)