Canonical Allele Identifier: CA1628076845

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50828698A= , CM000668.2:g.50828698A=	GRCh38
NC_000006.11:g.50796411A= , CM000668.1:g.50796411A=	GRCh37
NC_000006.10:g.50904370A=	NCBI36
NG_008438.1:g.14973A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000393655.4:c.601+19A= MANE Select	ENSP00000377265.2:n.601+19A=
ENST00000393655.3:c.601+19A=	ENSP00000377265.2:n.601+19A=
NM_003221.3:c.601+19A=	NP_003212.2:n.601+19A=
XM_006715176.2:c.601+19A=	XP_006715239.1:n.601+19A=
XM_006715177.2:c.547+19A=	XP_006715240.1:n.547+19A=
XM_011514834.1:c.628+19A=	XP_011513136.1:n.628+19A=
XM_011514835.1:c.628+19A=	XP_011513137.1:n.628+19A=
XM_011514836.1:c.628+19A=	XP_011513138.1:n.628+19A=
XM_011514837.1:c.628+19A=	XP_011513139.1:n.628+19A=
XM_011514837.2:c.628+19A=	XP_011513139.1:n.628+19A=
XM_017011233.1:c.766+19A=	XP_016866722.1:n.766+19A=
XM_017011234.1:c.730+19A=	XP_016866723.1:n.730+19A=
XM_017011235.2:c.142+19A=	XP_016866724.1:n.142+19A=
NM_003221.4:c.601+19A= MANE Select	NP_003212.2:n.601+19A=