Canonical Allele Identifier: CA2480601980
Gene: GATAD2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153816448G= , CM000663.2:g.153816448G= GRCh38
NC_000001.10:g.153788924G= , CM000663.1:g.153788924G= GRCh37
NC_000001.9:g.152055548G= NCBI36
NG_050988.1:g.111528C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703630.1:c.618C= ENSP00000515408.1:p.Asn206=
ENST00000368655.5:c.1041C= MANE Select ENSP00000357644.4:p.Asn347=
ENST00000368655.4:c.1041C= ENSP00000357644.4:p.Asn347=
ENST00000634408.1:c.993C= ENSP00000489595.1:p.Asn331=
ENST00000634544.1:c.1041C= ENSP00000489184.1:p.Asn347=
ENST00000634564.1:c.295C=
NM_020699.2:c.1041C= NP_065750.1:p.Asn347=
XM_005245364.3:c.1041C= XP_005245421.1:p.Asn347=
XM_006711469.2:c.1041C= XP_006711532.1:p.Asn347=
XM_011509808.1:c.1041C= XP_011508110.1:p.Asn347=
NM_020699.3:c.1041C= NP_065750.1:p.Asn347=
XM_005245364.4:c.1041C= XP_005245421.1:p.Asn347=
XM_024448621.1:c.1041C= XP_024304389.1:p.Asn347=
NM_020699.4:c.1041C= MANE Select NP_065750.1:p.Asn347=