Canonical Allele Identifier: CA1140415200
Gene: MIR29B2CHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207851475C= , CM000663.2:g.207851475C= GRCh38
NC_000001.10:g.208024820C= , CM000663.1:g.208024820C= GRCh37
NC_000001.9:g.206091443C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922491.1:n.143+16451G=