Canonical Allele Identifier: CA1628076670

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50828621A= , CM000668.2:g.50828621A=	GRCh38
NC_000006.11:g.50796334A= , CM000668.1:g.50796334A=	GRCh37
NC_000006.10:g.50904293A=	NCBI36
NG_008438.1:g.14896A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.543A= MANE Select	ENSP00000377265.2:p.Ser181=
ENST00000344788.7:c.537A=	ENSP00000342252.3:p.Ser179=
ENST00000393655.3:c.543A=	ENSP00000377265.2:p.Ser181=
NM_003221.3:c.543A=	NP_003212.2:p.Ser181=
XM_006715176.2:c.543A=	XP_006715239.1:p.Ser181=
XM_006715177.2:c.489A=	XP_006715240.1:p.Ser163=
XM_011514834.1:c.570A=	XP_011513136.1:p.Ser190=
XM_011514835.1:c.570A=	XP_011513137.1:p.Ser190=
XM_011514836.1:c.570A=	XP_011513138.1:p.Ser190=
XM_011514837.1:c.570A=	XP_011513139.1:p.Ser190=
XM_011514837.2:c.570A=	XP_011513139.1:p.Ser190=
XM_017011233.1:c.708A=	XP_016866722.1:p.Ser236=
XM_017011234.1:c.672A=	XP_016866723.1:p.Ser224=
XM_017011235.2:c.84A=	XP_016866724.1:p.Ser28=
NM_003221.4:c.543A= MANE Select	NP_003212.2:p.Ser181=