Canonical Allele Identifier: CA14450036

Gene: HOXB6 HOXB3 HOXB-AS3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.48596177C>T , CM000679.2:g.48596177C>T	GRCh38
NC_000017.10:g.46673539C>T , CM000679.1:g.46673539C>T	GRCh37
NC_000017.9:g.44028538C>T	NCBI36
NG_046953.1:g.13816G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018952.5:c.*236G>A (HOXB6) MANE Select	NP_061825.2:n.*236G>A
ENST00000225648.4:c.*236G>A (HOXB6) MANE Select	ENSP00000225648.3:n.*236G>A
NM_001369397.2:c.*236G>A (HOXB6)	NP_001356326.1:n.*236G>A
NM_018952.4:c.*236G>A (HOXB6)	NP_061825.2:n.*236G>A
NR_033201.2:n.170+5588C>T (HOXB-AS3)
NR_033202.2:n.171-4270C>T (HOXB-AS3)
NR_033203.1:n.73+3813C>T (HOXB-AS3)
NR_033204.2:n.73+3813C>T (HOXB-AS3)
NR_033205.1:n.166+54C>T (HOXB-AS3)
NR_110329.1:n.73+3813C>T (HOXB-AS3)
NR_110330.1:n.166+54C>T (HOXB-AS3)
NR_110331.1:n.171-4270C>T (HOXB-AS3)
ENST00000225648.3:c.*236G>A (HOXB6)	ENSP00000225648.3:n.*236G>A
ENST00000484302.3:c.*236G>A (HOXB6)	ENSP00000420009.2:n.*236G>A
ENST00000552000.2:n.433+8303G>A (HOXB3)
XM_005257283.2:c.*236G>A (HOXB6)	XP_005257340.1:n.*236G>A
XM_005257284.2:c.*236G>A (HOXB6)	XP_005257341.1:n.*236G>A
XM_005257284.3:c.*236G>A (HOXB6)	XP_005257341.1:n.*236G>A
XM_005257285.3:c.*236G>A (HOXB6)	XP_005257342.1:n.*236G>A
XM_006721856.2:c.*236G>A (HOXB6)	XP_006721919.1:n.*236G>A
XM_011524727.1:c.*236G>A (HOXB6)	XP_011523029.1:n.*236G>A
XM_011524727.3:c.*236G>A (HOXB6)	XP_011523029.1:n.*236G>A