Canonical Allele Identifier: CA1914325199
Gene: ARID5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61958499T= , CM000672.2:g.61958499T= GRCh38
NC_000010.10:g.63718258T= , CM000672.1:g.63718258T= GRCh37
NC_000010.9:g.63388264T= NCBI36
NG_030027.1:g.62246T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.502+18091T= MANE Select ENSP00000279873.7:n.502+18091T=
ENST00000644638.1:c.502+18091T= ENSP00000494412.1:n.502+18091T=
ENST00000681100.1:c.502+18091T= ENSP00000506119.1:n.502+18091T=
ENST00000279873.11:c.502+18091T= ENSP00000279873.7:n.502+18091T=
NM_032199.2:c.502+18091T= NP_115575.1:n.502+18091T=
XM_011540262.1:c.502+18091T= XP_011538564.1:n.502+18091T=
XM_024448230.1:c.-66+18091T= XP_024303998.1:n.-66+18091T=
NM_032199.3:c.502+18091T= MANE Select NP_115575.1:n.502+18091T=