Canonical Allele Identifier: CA400100449

Gene: HOXB3

Linked Data

• dbSNP Id: rs2229304
• MyVariant Identifiers: chr17:g.46629593G>A (hg19) ; chr17:g.48552231G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.48552231G>A , CM000679.2:g.48552231G>A	GRCh38
NC_000017.10:g.46629593G>A , CM000679.1:g.46629593G>A	GRCh37
NC_000017.9:g.43984592G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000498678.6:c.244C>T MANE Select	ENSP00000420595.1:p.Pro82Ser
ENST00000311626.8:c.244C>T	ENSP00000308252.4:p.Pro82Ser
ENST00000460160.5:c.-12-141C>T	ENSP00000418035.1:n.-12-141C>T
ENST00000470495.1:c.244C>T	ENSP00000417207.1:p.Pro82Ser
ENST00000471459.1:c.25C>T	ENSP00000417400.1:p.Pro9Ser
ENST00000472863.5:c.25C>T	ENSP00000419676.1:p.Pro9Ser
ENST00000476342.1:c.244C>T	ENSP00000418892.1:p.Pro82Ser
ENST00000489475.5:c.25C>T	ENSP00000418729.1:p.Pro9Ser
ENST00000490677.1:c.50-1053C>T	ENSP00000449977.1:n.50-1053C>T
ENST00000498678.5:c.244C>T	ENSP00000420595.1:p.Pro82Ser
NM_002146.4:c.244C>T	NP_002137.4:p.Pro82Ser
XM_005257277.3:c.244C>T	XP_005257334.1:p.Pro82Ser
XM_005257280.3:c.25C>T	XP_005257337.1:p.Pro9Ser
XM_005257282.3:c.-12-141C>T	XP_005257339.1:n.-12-141C>T
XM_006721854.2:c.244C>T	XP_006721917.1:p.Pro82Ser
XM_006721855.2:c.244C>T	XP_006721918.1:p.Pro82Ser
XM_011524707.1:c.685C>T	XP_011523009.1:p.Pro229Ser
XM_011524708.1:c.556-141C>T	XP_011523010.1:n.556-141C>T
XM_011524709.1:c.556-141C>T	XP_011523011.1:n.556-141C>T
XM_011524710.1:c.244C>T	XP_011523012.1:p.Pro82Ser
XM_011524711.1:c.244C>T	XP_011523013.1:p.Pro82Ser
XM_011524712.1:c.244C>T	XP_011523014.1:p.Pro82Ser
XM_011524713.1:c.244C>T	XP_011523015.1:p.Pro82Ser
XM_011524714.1:c.244C>T	XP_011523016.1:p.Pro82Ser
XM_011524715.1:c.244C>T	XP_011523017.1:p.Pro82Ser
XM_011524716.1:c.244C>T	XP_011523018.1:p.Pro82Ser
XM_011524717.1:c.244C>T	XP_011523019.1:p.Pro82Ser
XM_011524718.1:c.244C>T	XP_011523020.1:p.Pro82Ser
XM_011524719.1:c.244C>T	XP_011523021.1:p.Pro82Ser
XM_011524720.1:c.244C>T	XP_011523022.1:p.Pro82Ser
XM_011524721.1:c.244C>T	XP_011523023.1:p.Pro82Ser
XM_011524722.1:c.25C>T	XP_011523024.1:p.Pro9Ser
XM_011524723.1:c.-12-141C>T	XP_011523025.1:n.-12-141C>T
XM_011524724.1:c.-12-141C>T	XP_011523026.1:n.-12-141C>T
XM_011524725.1:c.620-141C>T	XP_011523027.1:n.620-141C>T
XM_011524726.1:c.25C>T	XP_011523028.1:p.Pro9Ser
NM_001330322.1:c.25C>T	NP_001317251.1:p.Pro9Ser
NM_001330323.1:c.-12-141C>T	NP_001317252.1:n.-12-141C>T
XM_006721854.3:c.244C>T	XP_006721917.1:p.Pro82Ser
XM_011524708.3:c.-12-141C>T	XP_011523010.2:n.-12-141C>T
XM_011524710.2:c.244C>T	XP_011523012.1:p.Pro82Ser
XM_011524719.2:c.244C>T	XP_011523021.1:p.Pro82Ser
XM_011524720.3:c.244C>T	XP_011523022.1:p.Pro82Ser
XM_011524721.3:c.244C>T	XP_011523023.1:p.Pro82Ser
XM_011524726.2:c.25C>T	XP_011523028.1:p.Pro9Ser
XM_017024560.1:c.685C>T	XP_016880049.1:p.Pro229Ser
XM_024450737.1:c.244C>T	XP_024306505.1:p.Pro82Ser
NM_001330322.2:c.25C>T	NP_001317251.1:p.Pro9Ser
NM_001384747.1:c.244C>T	NP_001371676.1:p.Pro82Ser
NM_001384749.1:c.244C>T MANE Select	NP_001371678.1:p.Pro82Ser
NM_001384750.1:c.25C>T	NP_001371679.1:p.Pro9Ser