Canonical Allele Identifier: CA364410085

Gene: TFAP2B

Linked Data

• MyVariant Identifiers: chr6:g.50786662G>T (hg19) ; chr6:g.50818949G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50818949G>T , CM000668.2:g.50818949G>T	GRCh38
NC_000006.11:g.50786662G>T , CM000668.1:g.50786662G>T	GRCh37
NC_000006.10:g.50894621G>T	NCBI36
NG_008438.1:g.5224G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000393655.4:c.58G>T MANE Select	ENSP00000377265.2:p.Val20Phe
ENST00000344788.7:c.25G>T	ENSP00000342252.3:p.Val9Phe
ENST00000393655.3:c.58G>T	ENSP00000377265.2:p.Val20Phe
NM_003221.3:c.58G>T	NP_003212.2:p.Val20Phe
XM_006715176.2:c.58G>T	XP_006715239.1:p.Val20Phe
XM_011514834.1:c.58G>T	XP_011513136.1:p.Val20Phe
XM_011514835.1:c.58G>T	XP_011513137.1:p.Val20Phe
XM_011514836.1:c.58G>T	XP_011513138.1:p.Val20Phe
XM_011514837.1:c.58G>T	XP_011513139.1:p.Val20Phe
XM_011514837.2:c.58G>T	XP_011513139.1:p.Val20Phe
XM_017011233.1:c.150G>T	XP_016866722.1:p.Met50Ile
XM_017011234.1:c.114G>T	XP_016866723.1:p.Met38Ile
XM_017011235.2:c.58G>T	XP_016866724.1:p.Val20Phe
NM_003221.4:c.58G>T MANE Select	NP_003212.2:p.Val20Phe