Canonical Allele Identifier: CA2711705952

Gene: TFAP2B

Linked Data

• dbSNP Id: rs2113938043

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50828695_50828696insTAATCTGACAG , CM000668.2:g.50828695_50828696insTAATCTGACAG	GRCh38
NC_000006.11:g.50796408_50796409insTAATCTGACAG , CM000668.1:g.50796408_50796409insTAATCTGACAG	GRCh37
NC_000006.10:g.50904367_50904368insTAATCTGACAG	NCBI36
NG_008438.1:g.14970_14971insTAATCTGACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.601+16_601+17insTAATCTGACAG MANE Select	ENSP00000377265.2:n.601+16_601+17insTAATCTGACAG
ENST00000393655.3:c.601+16_601+17insTAATCTGACAG	ENSP00000377265.2:n.601+16_601+17insTAATCTGACAG
NM_003221.3:c.601+16_601+17insTAATCTGACAG	NP_003212.2:n.601+16_601+17insTAATCTGACAG
XM_006715176.2:c.601+16_601+17insTAATCTGACAG	XP_006715239.1:n.601+16_601+17insTAATCTGACAG
XM_006715177.2:c.547+16_547+17insTAATCTGACAG	XP_006715240.1:n.547+16_547+17insTAATCTGACAG
XM_011514834.1:c.628+16_628+17insTAATCTGACAG	XP_011513136.1:n.628+16_628+17insTAATCTGACAG
XM_011514835.1:c.628+16_628+17insTAATCTGACAG	XP_011513137.1:n.628+16_628+17insTAATCTGACAG
XM_011514836.1:c.628+16_628+17insTAATCTGACAG	XP_011513138.1:n.628+16_628+17insTAATCTGACAG
XM_011514837.1:c.628+16_628+17insTAATCTGACAG	XP_011513139.1:n.628+16_628+17insTAATCTGACAG
XM_011514837.2:c.628+16_628+17insTAATCTGACAG	XP_011513139.1:n.628+16_628+17insTAATCTGACAG
XM_017011233.1:c.766+16_766+17insTAATCTGACAG	XP_016866722.1:n.766+16_766+17insTAATCTGACAG
XM_017011234.1:c.730+16_730+17insTAATCTGACAG	XP_016866723.1:n.730+16_730+17insTAATCTGACAG
XM_017011235.2:c.142+16_142+17insTAATCTGACAG	XP_016866724.1:n.142+16_142+17insTAATCTGACAG
NM_003221.4:c.601+16_601+17insTAATCTGACAG MANE Select	NP_003212.2:n.601+16_601+17insTAATCTGACAG