Canonical Allele Identifier: CA1914352044
Gene: ARID5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62020048C= , CM000672.2:g.62020048C= GRCh38
NC_000010.10:g.63779807C= , CM000672.1:g.63779807C= GRCh37
NC_000010.9:g.63449813C= NCBI36
NG_030027.1:g.123795C=

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.733+19727C= MANE Select ENSP00000279873.7:n.733+19727C=
ENST00000644638.1:c.734-4625C= ENSP00000494412.1:n.734-4625C=
ENST00000681100.1:c.733+19727C= ENSP00000506119.1:n.733+19727C=
ENST00000279873.11:c.733+19727C= ENSP00000279873.7:n.733+19727C=
NM_032199.2:c.733+19727C= NP_115575.1:n.733+19727C=
XM_011540262.1:c.503-30840C= XP_011538564.1:n.503-30840C=
XM_024448230.1:c.166+19727C= XP_024303998.1:n.166+19727C=
NM_032199.3:c.733+19727C= MANE Select NP_115575.1:n.733+19727C=