Canonical Allele Identifier: CA1628063507

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50818966C= , CM000668.2:g.50818966C=	GRCh38
NC_000006.11:g.50786679C= , CM000668.1:g.50786679C=	GRCh37
NC_000006.10:g.50894638C=	NCBI36
NG_008438.1:g.5241C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.75C= MANE Select	ENSP00000377265.2:p.Ile25=
ENST00000344788.7:c.42C=	ENSP00000342252.3:p.Ile14=
ENST00000393655.3:c.75C=	ENSP00000377265.2:p.Ile25=
NM_003221.3:c.75C=	NP_003212.2:p.Ile25=
XM_006715176.2:c.75C=	XP_006715239.1:p.Ile25=
XM_011514834.1:c.75C=	XP_011513136.1:p.Ile25=
XM_011514835.1:c.75C=	XP_011513137.1:p.Ile25=
XM_011514836.1:c.75C=	XP_011513138.1:p.Ile25=
XM_011514837.1:c.75C=	XP_011513139.1:p.Ile25=
XM_011514837.2:c.75C=	XP_011513139.1:p.Ile25=
XM_017011233.1:c.167C=	XP_016866722.1:p.Ser56=
XM_017011234.1:c.131C=	XP_016866723.1:p.Ser44=
XM_017011235.2:c.75C=	XP_016866724.1:p.Ile25=
NM_003221.4:c.75C= MANE Select	NP_003212.2:p.Ile25=