Canonical Allele Identifier: CA772629902
Gene: HOXB5 HGNC NCBI
HOXB3 HGNC NCBI
HOXB-AS3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48592068C>A , CM000679.2:g.48592068C>A GRCh38
NC_000017.10:g.46669430C>A , CM000679.1:g.46669430C>A GRCh37
NC_000017.9:g.44024429C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239151.6:c.*141G>T (HOXB5) MANE Select ENSP00000239151.4:n.*141G>T
ENST00000239151.5:c.*141G>T (HOXB5) ENSP00000239151.4:n.*141G>T
ENST00000552000.2:n.433+12412G>T (HOXB3)
NM_002147.3:c.*141G>T (HOXB5) NP_002138.1:n.*141G>T
NR_033201.2:n.170+1479C>A (HOXB-AS3)
NR_033202.2:n.170+1479C>A (HOXB-AS3)
NR_110331.1:n.170+1479C>A (HOXB-AS3)
NM_002147.4:c.*141G>T (HOXB5) MANE Select NP_002138.1:n.*141G>T
Search 100 bp 5'
Search 100 bp 3'