Canonical Allele Identifier: CA1628068361

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50823543C= , CM000668.2:g.50823543C=	GRCh38
NC_000006.11:g.50791256C= , CM000668.1:g.50791256C=	GRCh37
NC_000006.10:g.50899215C=	NCBI36
NG_008438.1:g.9818C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.218C= MANE Select	ENSP00000377265.2:p.Pro73=
ENST00000344788.7:c.212C=	ENSP00000342252.3:p.Pro71=
ENST00000393655.3:c.218C=	ENSP00000377265.2:p.Pro73=
ENST00000489228.1:n.513C=
NM_003221.3:c.218C=	NP_003212.2:p.Pro73=
XM_006715176.2:c.218C=	XP_006715239.1:p.Pro73=
XM_006715177.2:c.164C=	XP_006715240.1:p.Pro55=
XM_011514834.1:c.245C=	XP_011513136.1:p.Pro82=
XM_011514835.1:c.245C=	XP_011513137.1:p.Pro82=
XM_011514836.1:c.245C=	XP_011513138.1:p.Pro82=
XM_011514837.1:c.245C=	XP_011513139.1:p.Pro82=
XM_011514837.2:c.245C=	XP_011513139.1:p.Pro82=
XM_017011233.1:c.383C=	XP_016866722.1:p.Pro128=
XM_017011234.1:c.347C=	XP_016866723.1:p.Pro116=
XM_017011235.2:c.81+4571C=	XP_016866724.1:n.81+4571C=
NM_003221.4:c.218C= MANE Select	NP_003212.2:p.Pro73=