Canonical Allele Identifier: CA2263242626
Gene: HOXB13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728358G= , CM000679.2:g.48728358G= GRCh38
NC_000017.10:g.46805720G= , CM000679.1:g.46805720G= GRCh37
NC_000017.9:g.44160719G= NCBI36
NG_033789.1:g.5392C= , LRG_771:g.5392C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290295.8:c.236C= MANE Select ENSP00000290295.8:p.Pro79=
ENST00000290295.7:c.236C= ENSP00000290295.7:p.Pro79=
NM_006361.5:c.236C= , LRG_771t1:c.236C= NP_006352.2:p.Pro79=
NM_006361.6:c.236C= MANE Select NP_006352.2:p.Pro79=