Canonical Allele Identifier: CA2771023818
Gene: TFAP2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.50818846dup , CM000668.2:g.50818846dup GRCh38
NC_000006.11:g.50786559dup , CM000668.1:g.50786559dup GRCh37
NC_000006.10:g.50894518dup NCBI36
NG_008438.1:g.5121dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000344788.7:c.-79dup ENSP00000342252.3:n.-79dup
ENST00000393655.3:c.-46dup ENSP00000377265.2:n.-46dup
NM_003221.3:c.-46dup NP_003212.2:n.-46dup
XM_006715176.2:c.-46dup XP_006715239.1:n.-46dup
XM_011514834.1:c.-46dup XP_011513136.1:n.-46dup
XM_011514835.1:c.-46dup XP_011513137.1:n.-46dup
XM_011514836.1:c.-46dup XP_011513138.1:n.-46dup
XM_011514837.1:c.-46dup XP_011513139.1:n.-46dup
XM_011514837.2:c.-46dup XP_011513139.1:n.-46dup
XM_017011233.1:c.47dup XP_016866722.1:p.Tyr16Ter
XM_017011234.1:c.11dup XP_016866723.1:p.Tyr4Ter
XM_017011235.2:c.-46dup XP_016866724.1:n.-46dup