Canonical Allele Identifier: CA915950426
Gene: HOXB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 690717
ClinVar RCV Id: RCV000856020
dbSNP Id: rs1597934448

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728250del , CM000679.2:g.48728250del GRCh38
NC_000017.10:g.46805612del , CM000679.1:g.46805612del GRCh37
NC_000017.9:g.44160611del NCBI36
NG_033789.1:g.5500del , LRG_771:g.5500del

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.344del MANE Select ENSP00000290295.8:p.Thr115ArgfsTer?
ENST00000290295.7:c.344del ENSP00000290295.7:p.Thr115ArgfsTer?
NM_006361.5:c.344del , LRG_771t1:c.344del NP_006352.2:p.Thr115ArgfsTer?
NM_006361.6:c.344del MANE Select NP_006352.2:p.Thr115ArgfsTer?