Canonical Allele Identifier: CA2263242614
Gene: HOXB13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728344_48728345delinsCA , CM000679.2:g.48728344_48728345delinsCA GRCh38
NC_000017.10:g.46805706_46805707delinsCA , CM000679.1:g.46805706_46805707delinsCA GRCh37
NC_000017.9:g.44160705_44160706delinsCA NCBI36
NG_033789.1:g.5405_5406delinsTG , LRG_771:g.5405_5406delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.249_250delinsTG MANE Select ENSP00000290295.8:p.Phe83=
ENST00000290295.7:c.249_250delinsTG ENSP00000290295.7:p.Phe83=
NM_006361.5:c.249_250delinsTG , LRG_771t1:c.249_250delinsTG NP_006352.2:p.Phe83=
NM_006361.6:c.249_250delinsTG MANE Select NP_006352.2:p.Phe83=