Canonical Allele Identifier: CA915950442
Gene: HOXB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 690667
ClinVar RCV Id: RCV000855970
dbSNP Id: rs1597934671

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728347del , CM000679.2:g.48728347del GRCh38
NC_000017.10:g.46805709del , CM000679.1:g.46805709del GRCh37
NC_000017.9:g.44160708del NCBI36
NG_033789.1:g.5405del , LRG_771:g.5405del

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.249del MANE Select ENSP00000290295.8:p.Phe83LeufsTer15
ENST00000290295.7:c.249del ENSP00000290295.7:p.Phe83LeufsTer15
NM_006361.5:c.249del , LRG_771t1:c.249del NP_006352.2:p.Phe83LeufsTer15
NM_006361.6:c.249del MANE Select NP_006352.2:p.Phe83LeufsTer15