Canonical Allele Identifier: CA1628089037

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50838007G= , CM000668.2:g.50838007G=	GRCh38
NC_000006.11:g.50805720G= , CM000668.1:g.50805720G=	GRCh37
NC_000006.10:g.50913679G=	NCBI36
NG_008438.1:g.24282G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.854G= MANE Select	ENSP00000377265.2:p.Arg285=
ENST00000393655.3:c.854G=	ENSP00000377265.2:p.Arg285=
NM_003221.3:c.854G=	NP_003212.2:p.Arg285=
XM_006715176.2:c.854G=	XP_006715239.1:p.Arg285=
XM_006715177.2:c.800G=	XP_006715240.1:p.Arg267=
XM_011514834.1:c.881G=	XP_011513136.1:p.Arg294=
XM_011514835.1:c.881G=	XP_011513137.1:p.Arg294=
XM_011514836.1:c.881G=	XP_011513138.1:p.Arg294=
XM_011514837.1:c.881G=	XP_011513139.1:p.Arg294=
XM_011514837.2:c.881G=	XP_011513139.1:p.Arg294=
XM_017011233.1:c.1019G=	XP_016866722.1:p.Arg340=
XM_017011234.1:c.983G=	XP_016866723.1:p.Arg328=
XM_017011235.2:c.395G=	XP_016866724.1:p.Arg132=
NM_003221.4:c.854G= MANE Select	NP_003212.2:p.Arg285=