Canonical Allele Identifier: CA450411614

Gene: TFAP2B

Linked Data

• MyVariant Identifiers: chr6:g.50786658G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50818945G>A , CM000668.2:g.50818945G>A	GRCh38
NC_000006.11:g.50786658G>A , CM000668.1:g.50786658G>A	GRCh37
NC_000006.10:g.50894617G>A	NCBI36
NG_008438.1:g.5220G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.54G>A MANE Select	ENSP00000377265.2:p.Glu18=
ENST00000344788.7:c.21G>A	ENSP00000342252.3:p.Glu7=
ENST00000393655.3:c.54G>A	ENSP00000377265.2:p.Glu18=
NM_003221.3:c.54G>A	NP_003212.2:p.Glu18=
XM_006715176.2:c.54G>A	XP_006715239.1:p.Glu18=
XM_011514834.1:c.54G>A	XP_011513136.1:p.Glu18=
XM_011514835.1:c.54G>A	XP_011513137.1:p.Glu18=
XM_011514836.1:c.54G>A	XP_011513138.1:p.Glu18=
XM_011514837.1:c.54G>A	XP_011513139.1:p.Glu18=
XM_011514837.2:c.54G>A	XP_011513139.1:p.Glu18=
XM_017011233.1:c.146G>A	XP_016866722.1:p.Arg49Lys
XM_017011234.1:c.110G>A	XP_016866723.1:p.Arg37Lys
XM_017011235.2:c.54G>A	XP_016866724.1:p.Glu18=
NM_003221.4:c.54G>A MANE Select	NP_003212.2:p.Glu18=