Canonical Allele Identifier: CA2263242544
Gene: HOXB13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728262G= , CM000679.2:g.48728262G= GRCh38
NC_000017.10:g.46805624G= , CM000679.1:g.46805624G= GRCh37
NC_000017.9:g.44160623G= NCBI36
NG_033789.1:g.5488C= , LRG_771:g.5488C=

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.332C= MANE Select ENSP00000290295.8:p.Ala111=
ENST00000290295.7:c.332C= ENSP00000290295.7:p.Ala111=
NM_006361.5:c.332C= , LRG_771t1:c.332C= NP_006352.2:p.Ala111=
NM_006361.6:c.332C= MANE Select NP_006352.2:p.Ala111=