Canonical Allele Identifier: CA582821883

Gene: MIR2052HG LINC03071

Linked Data

• dbSNP Id: rs1196245754
• gnomAD v2: 8-75513041-C-T
• gnomAD v3: 8-74600806-C-T
• gnomAD v4: 8-74600806-C-T
• MyVariant Identifiers: chr8:g.75513041C>T (hg19) ; chr8:g.74600806C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74600806C>T , CM000670.2:g.74600806C>T	GRCh38
NC_000008.10:g.75513041C>T , CM000670.1:g.75513041C>T	GRCh37
NC_000008.9:g.75675596C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033830.1:n.43+898C>T (MIR2052HG)
XR_929054.1:n.459-10429G>A (LINC03071)
XR_929055.1:n.278-10429G>A (LINC03071)
XR_929057.1:n.336-10429G>A (LINC03071)
XR_001745957.1:n.742-10429G>A (LINC03071)
XR_001745958.1:n.561-10429G>A (LINC03071)
XR_001745960.1:n.336-10429G>A (LINC03071)