Canonical Allele Identifier: CA2679069789

Gene: TFAP2B

Linked Data

• gnomAD v4: 6-50819032-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50819032G>T , CM000668.2:g.50819032G>T	GRCh38
NC_000006.11:g.50786745G>T , CM000668.1:g.50786745G>T	GRCh37
NC_000006.10:g.50894704G>T	NCBI36
NG_008438.1:g.5307G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.81+60G>T MANE Select	ENSP00000377265.2:n.81+60G>T
ENST00000344788.7:c.48+60G>T	ENSP00000342252.3:n.48+60G>T
ENST00000393655.3:c.81+60G>T	ENSP00000377265.2:n.81+60G>T
NM_003221.3:c.81+60G>T	NP_003212.2:n.81+60G>T
XM_006715176.2:c.81+60G>T	XP_006715239.1:n.81+60G>T
XM_011514834.1:c.81+60G>T	XP_011513136.1:n.81+60G>T
XM_011514835.1:c.81+60G>T	XP_011513137.1:n.81+60G>T
XM_011514836.1:c.81+60G>T	XP_011513138.1:n.81+60G>T
XM_011514837.1:c.81+60G>T	XP_011513139.1:n.81+60G>T
XM_011514837.2:c.81+60G>T	XP_011513139.1:n.81+60G>T
XM_017011233.1:c.173+60G>T	XP_016866722.1:n.173+60G>T
XM_017011234.1:c.137+60G>T	XP_016866723.1:n.137+60G>T
XM_017011235.2:c.81+60G>T	XP_016866724.1:n.81+60G>T
NM_003221.4:c.81+60G>T MANE Select	NP_003212.2:n.81+60G>T