Canonical Allele Identifier: CA1628088987

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50837977C= , CM000668.2:g.50837977C=	GRCh38
NC_000006.11:g.50805690C= , CM000668.1:g.50805690C=	GRCh37
NC_000006.10:g.50913649C=	NCBI36
NG_008438.1:g.24252C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.824C= MANE Select	ENSP00000377265.2:p.Ala275=
ENST00000393655.3:c.824C=	ENSP00000377265.2:p.Ala275=
NM_003221.3:c.824C=	NP_003212.2:p.Ala275=
XM_006715176.2:c.824C=	XP_006715239.1:p.Ala275=
XM_006715177.2:c.770C=	XP_006715240.1:p.Ala257=
XM_011514834.1:c.851C=	XP_011513136.1:p.Ala284=
XM_011514835.1:c.851C=	XP_011513137.1:p.Ala284=
XM_011514836.1:c.851C=	XP_011513138.1:p.Ala284=
XM_011514837.1:c.851C=	XP_011513139.1:p.Ala284=
XM_011514837.2:c.851C=	XP_011513139.1:p.Ala284=
XM_017011233.1:c.989C=	XP_016866722.1:p.Ala330=
XM_017011234.1:c.953C=	XP_016866723.1:p.Ala318=
XM_017011235.2:c.365C=	XP_016866724.1:p.Ala122=
NM_003221.4:c.824C= MANE Select	NP_003212.2:p.Ala275=