Canonical Allele Identifier: CA2480603165
Gene: GATAD2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153819541T= , CM000663.2:g.153819541T= GRCh38
NC_000001.10:g.153792017T= , CM000663.1:g.153792017T= GRCh37
NC_000001.9:g.152058641T= NCBI36
NG_050988.1:g.108435A=

Transcript Alleles

HGVS Amino-acid change
ENST00000703630.1:c.42+65A= ENSP00000515408.1:n.42+65A=
ENST00000368655.5:c.465+65A= MANE Select ENSP00000357644.4:n.465+65A=
ENST00000368655.4:c.465+65A= ENSP00000357644.4:n.465+65A=
ENST00000634401.1:c.465+65A= ENSP00000489313.1:n.465+65A=
ENST00000634408.1:c.465+65A= ENSP00000489595.1:n.465+65A=
ENST00000634544.1:c.465+65A= ENSP00000489184.1:n.465+65A=
NM_020699.2:c.465+65A= NP_065750.1:n.465+65A=
XM_005245364.3:c.465+65A= XP_005245421.1:n.465+65A=
XM_006711469.2:c.465+65A= XP_006711532.1:n.465+65A=
XM_011509808.1:c.465+65A= XP_011508110.1:n.465+65A=
NM_020699.3:c.465+65A= NP_065750.1:n.465+65A=
XM_005245364.4:c.465+65A= XP_005245421.1:n.465+65A=
XM_024448621.1:c.465+65A= XP_024304389.1:n.465+65A=
NM_020699.4:c.465+65A= MANE Select NP_065750.1:n.465+65A=