Canonical Allele Identifier: CA340721

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50823543C>G , CM000668.2:g.50823543C>G	GRCh38
NC_000006.11:g.50791256C>G , CM000668.1:g.50791256C>G	GRCh37
NC_000006.10:g.50899215C>G	NCBI36
NG_008438.1:g.9818C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.218C>G MANE Select	ENSP00000377265.2:p.Pro73Arg
ENST00000344788.7:c.212C>G	ENSP00000342252.3:p.Pro71Arg
ENST00000393655.3:c.218C>G	ENSP00000377265.2:p.Pro73Arg
ENST00000489228.1:n.513C>G
NM_003221.3:c.218C>G	NP_003212.2:p.Pro73Arg
XM_006715176.2:c.218C>G	XP_006715239.1:p.Pro73Arg
XM_006715177.2:c.164C>G	XP_006715240.1:p.Pro55Arg
XM_011514834.1:c.245C>G	XP_011513136.1:p.Pro82Arg
XM_011514835.1:c.245C>G	XP_011513137.1:p.Pro82Arg
XM_011514836.1:c.245C>G	XP_011513138.1:p.Pro82Arg
XM_011514837.1:c.245C>G	XP_011513139.1:p.Pro82Arg
XM_011514837.2:c.245C>G	XP_011513139.1:p.Pro82Arg
XM_017011233.1:c.383C>G	XP_016866722.1:p.Pro128Arg
XM_017011234.1:c.347C>G	XP_016866723.1:p.Pro116Arg
XM_017011235.2:c.81+4571C>G	XP_016866724.1:n.81+4571C>G
NM_003221.4:c.218C>G MANE Select	NP_003212.2:p.Pro73Arg