Canonical Allele Identifier: CA1914373531
Gene: ARID5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62070527T= , CM000672.2:g.62070527T= GRCh38
NC_000010.10:g.63830286T= , CM000672.1:g.63830286T= GRCh37
NC_000010.9:g.63500292T= NCBI36
NG_030027.1:g.174274T=

Transcript Alleles

HGVS Amino-acid Change
NM_032199.3:c.1199+730T= MANE Select NP_115575.1:n.1199+730T=
ENST00000279873.12:c.1199+730T= MANE Select ENSP00000279873.7:n.1199+730T=
NM_001244638.1:c.470+730T= NP_001231567.1:n.470+730T=
NM_001244638.2:c.470+730T= NP_001231567.1:n.470+730T=
NM_032199.2:c.1199+730T= NP_115575.1:n.1199+730T=
ENST00000279873.11:c.1199+730T= ENSP00000279873.7:n.1199+730T=
ENST00000309334.5:c.470+730T= ENSP00000308862.5:n.470+730T=
ENST00000681100.1:c.1175+730T= ENSP00000506119.1:n.1175+730T=
XM_011540262.1:c.968+730T= XP_011538564.1:n.968+730T=
XM_024448230.1:c.632+730T= XP_024303998.1:n.632+730T=
XM_024448231.1:c.-278+730T= XP_024303999.1:n.-278+730T=