Canonical Allele Identifier: CA2263242618
Gene: HOXB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2066998
ClinVar RCV Id: RCV002943709
dbSNP Id: rs2038237526

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728351dup , CM000679.2:g.48728351dup GRCh38
NC_000017.10:g.46805713dup , CM000679.1:g.46805713dup GRCh37
NC_000017.9:g.44160712dup NCBI36
NG_033789.1:g.5400dup , LRG_771:g.5400dup

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.244dup MANE Select ENSP00000290295.8:p.Tyr82LeufsTer?
ENST00000290295.7:c.244dup ENSP00000290295.7:p.Tyr82LeufsTer?
NM_006361.5:c.244dup , LRG_771t1:c.244dup NP_006352.2:p.Tyr82LeufsTer?
NM_006361.6:c.244dup MANE Select NP_006352.2:p.Tyr82LeufsTer?