Canonical Allele Identifier: CA450411626

Gene: TFAP2B

Linked Data

• MyVariant Identifiers: chr6:g.50786664C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50818951C>T , CM000668.2:g.50818951C>T	GRCh38
NC_000006.11:g.50786664C>T , CM000668.1:g.50786664C>T	GRCh37
NC_000006.10:g.50894623C>T	NCBI36
NG_008438.1:g.5226C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.60C>T MANE Select	ENSP00000377265.2:p.Val20=
ENST00000344788.7:c.27C>T	ENSP00000342252.3:p.Val9=
ENST00000393655.3:c.60C>T	ENSP00000377265.2:p.Val20=
NM_003221.3:c.60C>T	NP_003212.2:p.Val20=
XM_006715176.2:c.60C>T	XP_006715239.1:p.Val20=
XM_011514834.1:c.60C>T	XP_011513136.1:p.Val20=
XM_011514835.1:c.60C>T	XP_011513137.1:p.Val20=
XM_011514836.1:c.60C>T	XP_011513138.1:p.Val20=
XM_011514837.1:c.60C>T	XP_011513139.1:p.Val20=
XM_011514837.2:c.60C>T	XP_011513139.1:p.Val20=
XM_017011233.1:c.152C>T	XP_016866722.1:p.Ser51Leu
XM_017011234.1:c.116C>T	XP_016866723.1:p.Ser39Leu
XM_017011235.2:c.60C>T	XP_016866724.1:p.Val20=
NM_003221.4:c.60C>T MANE Select	NP_003212.2:p.Val20=