Canonical Allele Identifier: CA1628065193

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50845193G= , CM000668.2:g.50845193G=	GRCh38
NC_000006.11:g.50812906G= , CM000668.1:g.50812906G=	GRCh37
NC_000006.10:g.50920865G=	NCBI36
NG_008438.1:g.31468G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.*1801G= MANE Select	ENSP00000377265.2:n.*1801G=
ENST00000393655.3:c.*1801G=	ENSP00000377265.2:n.*1801G=
NM_003221.3:c.*1801G=	NP_003212.2:n.*1801G=
XM_006715176.2:c.*740G=	XP_006715239.1:n.*740G=
XM_006715177.2:c.*740G=	XP_006715240.1:n.*740G=
XM_011514834.1:c.*740G=	XP_011513136.1:n.*740G=
XM_011514835.1:c.*740G=	XP_011513137.1:n.*740G=
XM_011514836.1:c.*2-508G=	XP_011513138.1:n.*2-508G=
XM_011514837.1:c.*1801G=	XP_011513139.1:n.*1801G=
XM_011514837.2:c.*1801G=	XP_011513139.1:n.*1801G=
XM_017011233.1:c.*1801G=	XP_016866722.1:n.*1801G=
XM_017011234.1:c.*1801G=	XP_016866723.1:n.*1801G=
XM_017011235.2:c.*1801G=	XP_016866724.1:n.*1801G=
NM_003221.4:c.*1801G= MANE Select	NP_003212.2:n.*1801G=