Canonical Allele Identifier: CA340716

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50837977C>A , CM000668.2:g.50837977C>A	GRCh38
NC_000006.11:g.50805690C>A , CM000668.1:g.50805690C>A	GRCh37
NC_000006.10:g.50913649C>A	NCBI36
NG_008438.1:g.24252C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.824C>A MANE Select	ENSP00000377265.2:p.Ala275Asp
ENST00000393655.3:c.824C>A	ENSP00000377265.2:p.Ala275Asp
NM_003221.3:c.824C>A	NP_003212.2:p.Ala275Asp
XM_006715176.2:c.824C>A	XP_006715239.1:p.Ala275Asp
XM_006715177.2:c.770C>A	XP_006715240.1:p.Ala257Asp
XM_011514834.1:c.851C>A	XP_011513136.1:p.Ala284Asp
XM_011514835.1:c.851C>A	XP_011513137.1:p.Ala284Asp
XM_011514836.1:c.851C>A	XP_011513138.1:p.Ala284Asp
XM_011514837.1:c.851C>A	XP_011513139.1:p.Ala284Asp
XM_011514837.2:c.851C>A	XP_011513139.1:p.Ala284Asp
XM_017011233.1:c.989C>A	XP_016866722.1:p.Ala330Asp
XM_017011234.1:c.953C>A	XP_016866723.1:p.Ala318Asp
XM_017011235.2:c.365C>A	XP_016866724.1:p.Ala122Asp
NM_003221.4:c.824C>A MANE Select	NP_003212.2:p.Ala275Asp