Canonical Allele Identifier: CA14512400
Gene: TAF4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.26312708G>A , CM000680.2:g.26312708G>A GRCh38
NC_000018.9:g.23892672G>A , CM000680.1:g.23892672G>A GRCh37
NC_000018.8:g.22146670G>A NCBI36
NG_034162.1:g.90826G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269142.10:c.1833-2521G>A MANE Select ENSP00000269142.6:n.1833-2521G>A
ENST00000269142.9:c.1833-2521G>A ENSP00000269142.5:n.1833-2521G>A
ENST00000400466.6:c.1842-2521G>A ENSP00000383314.3:n.1842-2521G>A
ENST00000418698.3:c.*96-2521G>A ENSP00000389365.3:n.*96-2521G>A
ENST00000578121.5:c.1848-2521G>A ENSP00000462980.1:n.1848-2521G>A
NM_001293725.1:c.1848-2521G>A NP_001280654.1:n.1848-2521G>A
NM_005640.2:c.1833-2521G>A NP_005631.1:n.1833-2521G>A
NR_121653.1:n.2004-2521G>A
XM_006722528.2:c.1833-2521G>A XP_006722591.2:n.1833-2521G>A
XM_011526153.1:c.1833-8362G>A XP_011524455.1:n.1833-8362G>A
XM_011526153.2:c.1833-8362G>A XP_011524455.1:n.1833-8362G>A
XM_017025932.1:c.1870-2521G>A XP_016881421.1:n.1870-2521G>A
XM_017025933.1:c.1071-2521G>A XP_016881422.1:n.1071-2521G>A
XM_024451239.1:c.1833-2521G>A XP_024307007.1:n.1833-2521G>A
NM_001293725.2:c.1848-2521G>A NP_001280654.1:n.1848-2521G>A
NM_005640.3:c.1833-2521G>A MANE Select NP_005631.1:n.1833-2521G>A
NR_121653.2:n.2442-2521G>A