Canonical Allele Identifier: CA1139905257
Gene: MIR29B2CHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207866126G= , CM000663.2:g.207866126G= GRCh38
NC_000001.10:g.208039471G= , CM000663.1:g.208039471G= GRCh37
NC_000001.9:g.206106094G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922491.1:n.143+1800C=