Canonical Allele Identifier: CA179762221
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Linked Data

dbSNP Id: rs1005672999
MyVariant Identifiers: chr8:g.75527510T>C (hg19) chr8:g.74615275T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74615275T>C , CM000670.2:g.74615275T>C GRCh38
NC_000008.10:g.75527510T>C , CM000670.1:g.75527510T>C GRCh37
NC_000008.9:g.75690065T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.131+2335T>C (MIR2052HG)
XR_929054.1:n.345+1485A>G (LINC03071)
XR_929055.1:n.165-2709A>G (LINC03071)
XR_929056.1:n.345+1485A>G (LINC03071)
XR_929057.1:n.222+1485A>G (LINC03071)
XR_001745957.1:n.628+1485A>G (LINC03071)
XR_001745958.1:n.448-2709A>G (LINC03071)
XR_001745960.1:n.222+1485A>G (LINC03071)
XR_002956714.1:n.628+1485A>G (LINC03071)
Search 100 bp 5'
Search 100 bp 3'