Canonical Allele Identifier: CA1140119246

Gene: GATAD2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153876520G= , CM000663.2:g.153876520G=	GRCh38
NC_000001.10:g.153848996G= , CM000663.1:g.153848996G=	GRCh37
NC_000001.9:g.152115620G=	NCBI36
NG_050988.1:g.51456C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020699.4:c.-2+46213C= MANE Select	NP_065750.1:n.-2+46213C=
ENST00000368655.5:c.-2+46213C= MANE Select	ENSP00000357644.4:n.-2+46213C=
NM_020699.2:c.-2+46213C=	NP_065750.1:n.-2+46213C=
NM_020699.3:c.-2+46213C=	NP_065750.1:n.-2+46213C=
ENST00000368655.4:c.-2+46213C=	ENSP00000357644.4:n.-2+46213C=
ENST00000634401.1:c.-2+38154C=	ENSP00000489313.1:n.-2+38154C=
ENST00000634408.1:c.-2+46213C=	ENSP00000489595.1:n.-2+46213C=
ENST00000634544.1:c.-2+45319C=	ENSP00000489184.1:n.-2+45319C=
ENST00000634791.1:c.-2+9904C=	ENSP00000489566.1:n.-2+9904C=
ENST00000636014.1:n.96+22336C=
ENST00000637331.1:c.-2+46779C=	ENSP00000490635.1:n.-2+46779C=
ENST00000703630.1:c.-89+46213C=	ENSP00000515408.1:n.-89+46213C=
XM_005245364.3:c.-2+16786C=	XP_005245421.1:n.-2+16786C=
XM_005245364.4:c.-2+16786C=	XP_005245421.1:n.-2+16786C=
XM_011509808.1:c.-2+22336C=	XP_011508110.1:n.-2+22336C=
XM_024448621.1:c.-2+46779C=	XP_024304389.1:n.-2+46779C=