Canonical Allele Identifier: CA1914314662
Gene: ARID5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61935146G= , CM000672.2:g.61935146G= GRCh38
NC_000010.10:g.63694905G= , CM000672.1:g.63694905G= GRCh37
NC_000010.9:g.63364911G= NCBI36
NG_030027.1:g.38893G=

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.277-5037G= MANE Select ENSP00000279873.7:n.277-5037G=
ENST00000644638.1:c.277-5037G= ENSP00000494412.1:n.277-5037G=
ENST00000681100.1:c.277-5037G= ENSP00000506119.1:n.277-5037G=
ENST00000279873.11:c.277-5037G= ENSP00000279873.7:n.277-5037G=
NM_032199.2:c.277-5037G= NP_115575.1:n.277-5037G=
XM_011540262.1:c.277-5037G= XP_011538564.1:n.277-5037G=
XM_024448230.1:c.-291-5037G= XP_024303998.1:n.-291-5037G=
NM_032199.3:c.277-5037G= MANE Select NP_115575.1:n.277-5037G=