Canonical Allele Identifier: CA1914337292
Gene: ARID5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61985860A= , CM000672.2:g.61985860A= GRCh38
NC_000010.10:g.63745619A= , CM000672.1:g.63745619A= GRCh37
NC_000010.9:g.63415625A= NCBI36
NG_030027.1:g.89607A=

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.503-14231A= MANE Select ENSP00000279873.7:n.503-14231A=
ENST00000644638.1:c.503-14231A= ENSP00000494412.1:n.503-14231A=
ENST00000681100.1:c.503-14231A= ENSP00000506119.1:n.503-14231A=
ENST00000279873.11:c.503-14231A= ENSP00000279873.7:n.503-14231A=
NM_032199.2:c.503-14231A= NP_115575.1:n.503-14231A=
XM_011540262.1:c.502+45452A= XP_011538564.1:n.502+45452A=
XM_024448230.1:c.-65-14231A= XP_024303998.1:n.-65-14231A=
NM_032199.3:c.503-14231A= MANE Select NP_115575.1:n.503-14231A=