Canonical Allele Identifier: CA1115372996

Gene: MIR2052HG LINC03071

Linked Data

• dbSNP Id: rs1808265329
• gnomAD v3: 8-74615400-A-G
• gnomAD v4: 8-74615400-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74615400A>G , CM000670.2:g.74615400A>G	GRCh38
NC_000008.10:g.75527635A>G , CM000670.1:g.75527635A>G	GRCh37
NC_000008.9:g.75690190A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033830.1:n.131+2460A>G (MIR2052HG)
XR_929054.1:n.345+1360T>C (LINC03071)
XR_929055.1:n.165-2834T>C (LINC03071)
XR_929056.1:n.345+1360T>C (LINC03071)
XR_929057.1:n.222+1360T>C (LINC03071)
XR_001745957.1:n.628+1360T>C (LINC03071)
XR_001745958.1:n.448-2834T>C (LINC03071)
XR_001745960.1:n.222+1360T>C (LINC03071)
XR_002956714.1:n.628+1360T>C (LINC03071)