Canonical Allele Identifier: CA2263242612
Gene: HOXB13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728342_48728343delinsTC , CM000679.2:g.48728342_48728343delinsTC GRCh38
NC_000017.10:g.46805704_46805705delinsTC , CM000679.1:g.46805704_46805705delinsTC GRCh37
NC_000017.9:g.44160703_44160704delinsTC NCBI36
NG_033789.1:g.5407_5408delinsGA , LRG_771:g.5407_5408delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.251_252delinsGA MANE Select ENSP00000290295.8:p.Gly84=
ENST00000290295.7:c.251_252delinsGA ENSP00000290295.7:p.Gly84=
NM_006361.5:c.251_252delinsGA , LRG_771t1:c.251_252delinsGA NP_006352.2:p.Gly84=
NM_006361.6:c.251_252delinsGA MANE Select NP_006352.2:p.Gly84=