Canonical Allele Identifier: CA1628086572

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50836165C= , CM000668.2:g.50836165C=	GRCh38
NC_000006.11:g.50803878C= , CM000668.1:g.50803878C=	GRCh37
NC_000006.10:g.50911837C=	NCBI36
NG_008438.1:g.22440C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.706C= MANE Select	ENSP00000377265.2:p.Arg236=
ENST00000393655.3:c.706C=	ENSP00000377265.2:p.Arg236=
NM_003221.3:c.706C=	NP_003212.2:p.Arg236=
XM_006715176.2:c.706C=	XP_006715239.1:p.Arg236=
XM_006715177.2:c.652C=	XP_006715240.1:p.Arg218=
XM_011514834.1:c.733C=	XP_011513136.1:p.Arg245=
XM_011514835.1:c.733C=	XP_011513137.1:p.Arg245=
XM_011514836.1:c.733C=	XP_011513138.1:p.Arg245=
XM_011514837.1:c.733C=	XP_011513139.1:p.Arg245=
XM_011514837.2:c.733C=	XP_011513139.1:p.Arg245=
XM_017011233.1:c.871C=	XP_016866722.1:p.Arg291=
XM_017011234.1:c.835C=	XP_016866723.1:p.Arg279=
XM_017011235.2:c.247C=	XP_016866724.1:p.Arg83=
NM_003221.4:c.706C= MANE Select	NP_003212.2:p.Arg236=