Canonical Allele Identifier: CA1141830216

Gene: ZBTB7B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155015228C= , CM000663.2:g.155015228C=	GRCh38
NC_000001.10:g.154987704C= , CM000663.1:g.154987704C=	GRCh37
NC_000001.9:g.153254328C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535420.6:c.568C= MANE Select	ENSP00000438647.1:p.Pro190=
ENST00000292176.2:c.568C=	ENSP00000292176.2:p.Pro190=
ENST00000368426.3:c.568C=	ENSP00000357411.3:p.Pro190=
ENST00000417934.6:c.670C=	ENSP00000406286.2:p.Pro224=
ENST00000487542.1:n.792C=
ENST00000535420.5:c.568C=	ENSP00000438647.1:p.Pro190=
NM_001252406.2:c.670C=	NP_001239335.1:p.Pro224=
NM_001256455.1:c.568C=	NP_001243384.1:p.Pro190=
NR_045515.1:n.955C=
NR_046206.1:n.811C=
NR_049765.1:n.732C=
XM_006711349.2:c.568C=	XP_006711412.2:p.Pro190=
XM_006711353.1:c.568C=	XP_006711416.1:p.Pro190=
XM_006711354.1:c.568C=	XP_006711417.1:p.Pro190=
XM_006711356.2:c.568C=	XP_006711419.1:p.Pro190=
XM_006711357.1:c.568C=	XP_006711420.1:p.Pro190=
XM_006711358.1:c.568C=	XP_006711421.1:p.Pro190=
XM_006711359.1:c.568C=	XP_006711422.1:p.Pro190=
XM_011509598.1:c.670C=	XP_011507900.1:p.Pro224=
XM_011509599.1:c.568C=	XP_011507901.1:p.Pro190=
XM_006711356.3:c.568C=	XP_006711419.1:p.Pro190=
XM_006711359.2:c.568C=	XP_006711422.1:p.Pro190=
XM_011509598.2:c.670C=	XP_011507900.1:p.Pro224=
XM_011509599.2:c.568C=	XP_011507901.1:p.Pro190=
XM_017001399.1:c.841C=	XP_016856888.1:p.Pro281=
NM_001252406.3:c.670C=	NP_001239335.1:p.Pro224=
NM_001256455.2:c.568C= MANE Select	NP_001243384.1:p.Pro190=
NM_001377451.1:c.670C=	NP_001364380.1:p.Pro224=
NM_001377452.1:c.568C=	NP_001364381.1:p.Pro190=
NM_001377453.1:c.568C=	NP_001364382.1:p.Pro190=
NM_001377454.1:c.568C=	NP_001364383.1:p.Pro190=
NM_001377455.1:c.568C=	NP_001364384.1:p.Pro190=