Canonical Allele Identifier: CA2263242628
Gene: HOXB13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728360C= , CM000679.2:g.48728360C= GRCh38
NC_000017.10:g.46805722C= , CM000679.1:g.46805722C= GRCh37
NC_000017.9:g.44160721C= NCBI36
NG_033789.1:g.5390G= , LRG_771:g.5390G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290295.8:c.234G= MANE Select ENSP00000290295.8:p.Val78=
ENST00000290295.7:c.234G= ENSP00000290295.7:p.Val78=
NM_006361.5:c.234G= , LRG_771t1:c.234G= NP_006352.2:p.Val78=
NM_006361.6:c.234G= MANE Select NP_006352.2:p.Val78=