Canonical Allele Identifier: CA179762222

Gene: MIR2052HG LINC03071

Linked Data

• dbSNP Id: rs561763245
• gnomAD v2: 8-75527541-T-C
• gnomAD v3: 8-74615306-T-C
• gnomAD v4: 8-74615306-T-C
• MyVariant Identifiers: chr8:g.75527541T>C (hg19) ; chr8:g.74615306T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.74615306T>C , CM000670.2:g.74615306T>C	GRCh38
NC_000008.10:g.75527541T>C , CM000670.1:g.75527541T>C	GRCh37
NC_000008.9:g.75690096T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033830.1:n.131+2366T>C (MIR2052HG)
XR_929054.1:n.345+1454A>G (LINC03071)
XR_929055.1:n.165-2740A>G (LINC03071)
XR_929056.1:n.345+1454A>G (LINC03071)
XR_929057.1:n.222+1454A>G (LINC03071)
XR_001745957.1:n.628+1454A>G (LINC03071)
XR_001745958.1:n.448-2740A>G (LINC03071)
XR_001745960.1:n.222+1454A>G (LINC03071)
XR_002956714.1:n.628+1454A>G (LINC03071)