Canonical Allele Identifier: CA340718

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50836165C>T , CM000668.2:g.50836165C>T	GRCh38
NC_000006.11:g.50803878C>T , CM000668.1:g.50803878C>T	GRCh37
NC_000006.10:g.50911837C>T	NCBI36
NG_008438.1:g.22440C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.706C>T MANE Select	ENSP00000377265.2:p.Arg236Cys
ENST00000393655.3:c.706C>T	ENSP00000377265.2:p.Arg236Cys
NM_003221.3:c.706C>T	NP_003212.2:p.Arg236Cys
XM_006715176.2:c.706C>T	XP_006715239.1:p.Arg236Cys
XM_006715177.2:c.652C>T	XP_006715240.1:p.Arg218Cys
XM_011514834.1:c.733C>T	XP_011513136.1:p.Arg245Cys
XM_011514835.1:c.733C>T	XP_011513137.1:p.Arg245Cys
XM_011514836.1:c.733C>T	XP_011513138.1:p.Arg245Cys
XM_011514837.1:c.733C>T	XP_011513139.1:p.Arg245Cys
XM_011514837.2:c.733C>T	XP_011513139.1:p.Arg245Cys
XM_017011233.1:c.871C>T	XP_016866722.1:p.Arg291Cys
XM_017011234.1:c.835C>T	XP_016866723.1:p.Arg279Cys
XM_017011235.2:c.247C>T	XP_016866724.1:p.Arg83Cys
NM_003221.4:c.706C>T MANE Select	NP_003212.2:p.Arg236Cys