Canonical Allele Identifier: CA2263242536
Gene: HOXB13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728249_48728250delinsCG , CM000679.2:g.48728249_48728250delinsCG GRCh38
NC_000017.10:g.46805611_46805612delinsCG , CM000679.1:g.46805611_46805612delinsCG GRCh37
NC_000017.9:g.44160610_44160611delinsCG NCBI36
NG_033789.1:g.5500_5501delinsCG , LRG_771:g.5500_5501delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.344_345delinsCG MANE Select ENSP00000290295.8:p.Thr115=
ENST00000290295.7:c.344_345delinsCG ENSP00000290295.7:p.Thr115=
NM_006361.5:c.344_345delinsCG , LRG_771t1:c.344_345delinsCG NP_006352.2:p.Thr115=
NM_006361.6:c.344_345delinsCG MANE Select NP_006352.2:p.Thr115=