Canonical Allele Identifier: CA364410170

Gene: TFAP2B

Linked Data

• MyVariant Identifiers: chr6:g.50786671G>T (hg19) ; chr6:g.50818958G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50818958G>T , CM000668.2:g.50818958G>T	GRCh38
NC_000006.11:g.50786671G>T , CM000668.1:g.50786671G>T	GRCh37
NC_000006.10:g.50894630G>T	NCBI36
NG_008438.1:g.5233G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.67G>T MANE Select	ENSP00000377265.2:p.Glu23Ter
ENST00000344788.7:c.34G>T	ENSP00000342252.3:p.Glu12Ter
ENST00000393655.3:c.67G>T	ENSP00000377265.2:p.Glu23Ter
NM_003221.3:c.67G>T	NP_003212.2:p.Glu23Ter
XM_006715176.2:c.67G>T	XP_006715239.1:p.Glu23Ter
XM_011514834.1:c.67G>T	XP_011513136.1:p.Glu23Ter
XM_011514835.1:c.67G>T	XP_011513137.1:p.Glu23Ter
XM_011514836.1:c.67G>T	XP_011513138.1:p.Glu23Ter
XM_011514837.1:c.67G>T	XP_011513139.1:p.Glu23Ter
XM_011514837.2:c.67G>T	XP_011513139.1:p.Glu23Ter
XM_017011233.1:c.159G>T	XP_016866722.1:p.Thr53=
XM_017011234.1:c.123G>T	XP_016866723.1:p.Thr41=
XM_017011235.2:c.67G>T	XP_016866724.1:p.Glu23Ter
NM_003221.4:c.67G>T MANE Select	NP_003212.2:p.Glu23Ter