Canonical Allele Identifier: CA2631848396
Gene: MIR193BHG HGNC NCBI

Linked Data

dbSNP Id: rs2151509720

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.14301576G>A , CM000678.2:g.14301576G>A GRCh38
NC_000016.9:g.14395433G>A , CM000678.1:g.14395433G>A GRCh37
NC_000016.8:g.14302934G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_170633.1:n.151+45G>A