Canonical Allele Identifier: CA915950441
Gene: HOXB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 690670
ClinVar RCV Id: RCV000855973
dbSNP Id: rs1597934667

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728344del , CM000679.2:g.48728344del GRCh38
NC_000017.10:g.46805706del , CM000679.1:g.46805706del GRCh37
NC_000017.9:g.44160705del NCBI36
NG_033789.1:g.5407del , LRG_771:g.5407del

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.251del MANE Select ENSP00000290295.8:p.Gly84GlufsTer14
ENST00000290295.7:c.251del ENSP00000290295.7:p.Gly84GlufsTer14
NM_006361.5:c.251del , LRG_771t1:c.251del NP_006352.2:p.Gly84GlufsTer14
NM_006361.6:c.251del MANE Select NP_006352.2:p.Gly84GlufsTer14