Canonical Allele Identifier: CA2679069770

Gene: TFAP2B

Linked Data

• gnomAD v4: 6-50818859-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50818861del , CM000668.2:g.50818861del	GRCh38
NC_000006.11:g.50786574del , CM000668.1:g.50786574del	GRCh37
NC_000006.10:g.50894533del	NCBI36
NG_008438.1:g.5136del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344788.7:c.-64del	ENSP00000342252.3:n.-64del
ENST00000393655.3:c.-31del	ENSP00000377265.2:n.-31del
NM_003221.3:c.-31del	NP_003212.2:n.-31del
XM_006715176.2:c.-31del	XP_006715239.1:n.-31del
XM_011514834.1:c.-31del	XP_011513136.1:n.-31del
XM_011514835.1:c.-31del	XP_011513137.1:n.-31del
XM_011514836.1:c.-31del	XP_011513138.1:n.-31del
XM_011514837.1:c.-31del	XP_011513139.1:n.-31del
XM_011514837.2:c.-31del	XP_011513139.1:n.-31del
XM_017011233.1:c.62del	XP_016866722.1:p.Pro21LeufsTer16
XM_017011234.1:c.26del	XP_016866723.1:p.Pro9LeufsTer16
XM_017011235.2:c.-31del	XP_016866724.1:n.-31del