Canonical Allele Identifier: CA2480603188

Gene: GATAD2B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153819578G= , CM000663.2:g.153819578G=	GRCh38
NC_000001.10:g.153792054G= , CM000663.1:g.153792054G=	GRCh37
NC_000001.9:g.152058678G=	NCBI36
NG_050988.1:g.108398C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703630.1:c.42+28C=	ENSP00000515408.1:n.42+28C=
ENST00000368655.5:c.465+28C= MANE Select	ENSP00000357644.4:n.465+28C=
ENST00000368655.4:c.465+28C=	ENSP00000357644.4:n.465+28C=
ENST00000634401.1:c.465+28C=	ENSP00000489313.1:n.465+28C=
ENST00000634408.1:c.465+28C=	ENSP00000489595.1:n.465+28C=
ENST00000634544.1:c.465+28C=	ENSP00000489184.1:n.465+28C=
NM_020699.2:c.465+28C=	NP_065750.1:n.465+28C=
XM_005245364.3:c.465+28C=	XP_005245421.1:n.465+28C=
XM_006711469.2:c.465+28C=	XP_006711532.1:n.465+28C=
XM_011509808.1:c.465+28C=	XP_011508110.1:n.465+28C=
NM_020699.3:c.465+28C=	NP_065750.1:n.465+28C=
XM_005245364.4:c.465+28C=	XP_005245421.1:n.465+28C=
XM_024448621.1:c.465+28C=	XP_024304389.1:n.465+28C=
NM_020699.4:c.465+28C= MANE Select	NP_065750.1:n.465+28C=