Canonical Allele Identifier: CA2263242543

Gene: HOXB13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.48728261C= , CM000679.2:g.48728261C=	GRCh38
NC_000017.10:g.46805623C= , CM000679.1:g.46805623C=	GRCh37
NC_000017.9:g.44160622C=	NCBI36
NG_033789.1:g.5489G= , LRG_771:g.5489G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290295.8:c.333G= MANE Select	ENSP00000290295.8:p.Ala111=
ENST00000290295.7:c.333G=	ENSP00000290295.7:p.Ala111=
NM_006361.5:c.333G= , LRG_771t1:c.333G=	NP_006352.2:p.Ala111=
NM_006361.6:c.333G= MANE Select	NP_006352.2:p.Ala111=