Canonical Allele Identifier: CA2733710640
Gene: HOXB13 HGNC NCBI

Linked Data

dbSNP Id: rs2143073507

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728353del , CM000679.2:g.48728353del GRCh38
NC_000017.10:g.46805715del , CM000679.1:g.46805715del GRCh37
NC_000017.9:g.44160714del NCBI36
NG_033789.1:g.5398del , LRG_771:g.5398del

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.242del MANE Select ENSP00000290295.8:p.Gly81ValfsTer17
ENST00000290295.7:c.242del ENSP00000290295.7:p.Gly81ValfsTer17
NM_006361.5:c.242del , LRG_771t1:c.242del NP_006352.2:p.Gly81ValfsTer17
NM_006361.6:c.242del MANE Select NP_006352.2:p.Gly81ValfsTer17