Canonical Allele Identifier: CA2263242539

Gene: HOXB13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.48728254G= , CM000679.2:g.48728254G=	GRCh38
NC_000017.10:g.46805616G= , CM000679.1:g.46805616G=	GRCh37
NC_000017.9:g.44160615G=	NCBI36
NG_033789.1:g.5496C= , LRG_771:g.5496C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290295.8:c.340C= MANE Select	ENSP00000290295.8:p.Pro114=
ENST00000290295.7:c.340C=	ENSP00000290295.7:p.Pro114=
NM_006361.5:c.340C= , LRG_771t1:c.340C=	NP_006352.2:p.Pro114=
NM_006361.6:c.340C= MANE Select	NP_006352.2:p.Pro114=