Canonical Allele Identifier: CA364413744

Gene: TFAP2B

Linked Data

• MyVariant Identifiers: chr6:g.50796333C>A (hg19) ; chr6:g.50828620C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50828620C>A , CM000668.2:g.50828620C>A	GRCh38
NC_000006.11:g.50796333C>A , CM000668.1:g.50796333C>A	GRCh37
NC_000006.10:g.50904292C>A	NCBI36
NG_008438.1:g.14895C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.542C>A MANE Select	ENSP00000377265.2:p.Ser181Ter
ENST00000344788.7:c.536C>A	ENSP00000342252.3:p.Ser179Ter
ENST00000393655.3:c.542C>A	ENSP00000377265.2:p.Ser181Ter
NM_003221.3:c.542C>A	NP_003212.2:p.Ser181Ter
XM_006715176.2:c.542C>A	XP_006715239.1:p.Ser181Ter
XM_006715177.2:c.488C>A	XP_006715240.1:p.Ser163Ter
XM_011514834.1:c.569C>A	XP_011513136.1:p.Ser190Ter
XM_011514835.1:c.569C>A	XP_011513137.1:p.Ser190Ter
XM_011514836.1:c.569C>A	XP_011513138.1:p.Ser190Ter
XM_011514837.1:c.569C>A	XP_011513139.1:p.Ser190Ter
XM_011514837.2:c.569C>A	XP_011513139.1:p.Ser190Ter
XM_017011233.1:c.707C>A	XP_016866722.1:p.Ser236Ter
XM_017011234.1:c.671C>A	XP_016866723.1:p.Ser224Ter
XM_017011235.2:c.83C>A	XP_016866724.1:p.Ser28Ter
NM_003221.4:c.542C>A MANE Select	NP_003212.2:p.Ser181Ter