Canonical Allele Identifier: CA2679069796

Gene: TFAP2B

Linked Data

• gnomAD v4: 6-50819041-A-AATG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50819044_50819046dup , CM000668.2:g.50819044_50819046dup	GRCh38
NC_000006.11:g.50786757_50786759dup , CM000668.1:g.50786757_50786759dup	GRCh37
NC_000006.10:g.50894716_50894718dup	NCBI36
NG_008438.1:g.5319_5321dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.81+72_81+74dup MANE Select	ENSP00000377265.2:n.81+72_81+74dup
ENST00000344788.7:c.48+72_48+74dup	ENSP00000342252.3:n.48+72_48+74dup
ENST00000393655.3:c.81+72_81+74dup	ENSP00000377265.2:n.81+72_81+74dup
NM_003221.3:c.81+72_81+74dup	NP_003212.2:n.81+72_81+74dup
XM_006715176.2:c.81+72_81+74dup	XP_006715239.1:n.81+72_81+74dup
XM_011514834.1:c.81+72_81+74dup	XP_011513136.1:n.81+72_81+74dup
XM_011514835.1:c.81+72_81+74dup	XP_011513137.1:n.81+72_81+74dup
XM_011514836.1:c.81+72_81+74dup	XP_011513138.1:n.81+72_81+74dup
XM_011514837.1:c.81+72_81+74dup	XP_011513139.1:n.81+72_81+74dup
XM_011514837.2:c.81+72_81+74dup	XP_011513139.1:n.81+72_81+74dup
XM_017011233.1:c.173+72_173+74dup	XP_016866722.1:n.173+72_173+74dup
XM_017011234.1:c.137+72_137+74dup	XP_016866723.1:n.137+72_137+74dup
XM_017011235.2:c.81+72_81+74dup	XP_016866724.1:n.81+72_81+74dup
NM_003221.4:c.81+72_81+74dup MANE Select	NP_003212.2:n.81+72_81+74dup