Canonical Allele Identifier: CA2263242540

Gene: HOXB13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.48728256G= , CM000679.2:g.48728256G=	GRCh38
NC_000017.10:g.46805618G= , CM000679.1:g.46805618G=	GRCh37
NC_000017.9:g.44160617G=	NCBI36
NG_033789.1:g.5494C= , LRG_771:g.5494C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000290295.8:c.338C= MANE Select	ENSP00000290295.8:p.Thr113=
ENST00000290295.7:c.338C=	ENSP00000290295.7:p.Thr113=
NM_006361.5:c.338C= , LRG_771t1:c.338C=	NP_006352.2:p.Thr113=
NM_006361.6:c.338C= MANE Select	NP_006352.2:p.Thr113=