Canonical Allele Identifier: CA1914327465
Gene: ARID5B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61963700G= , CM000672.2:g.61963700G= GRCh38
NC_000010.10:g.63723459G= , CM000672.1:g.63723459G= GRCh37
NC_000010.9:g.63393465G= NCBI36
NG_030027.1:g.67447G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.502+23292G= MANE Select ENSP00000279873.7:n.502+23292G=
ENST00000644638.1:c.502+23292G= ENSP00000494412.1:n.502+23292G=
ENST00000681100.1:c.502+23292G= ENSP00000506119.1:n.502+23292G=
ENST00000279873.11:c.502+23292G= ENSP00000279873.7:n.502+23292G=
NM_032199.2:c.502+23292G= NP_115575.1:n.502+23292G=
XM_011540262.1:c.502+23292G= XP_011538564.1:n.502+23292G=
XM_024448230.1:c.-66+23292G= XP_024303998.1:n.-66+23292G=
NM_032199.3:c.502+23292G= MANE Select NP_115575.1:n.502+23292G=
Search 100 bp 5'
Search 100 bp 3'