Canonical Allele Identifier: CA1914325182

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61958459_61958460delinsCT , CM000672.2:g.61958459_61958460delinsCT	GRCh38
NC_000010.10:g.63718218_63718219delinsCT , CM000672.1:g.63718218_63718219delinsCT	GRCh37
NC_000010.9:g.63388224_63388225delinsCT	NCBI36
NG_030027.1:g.62206_62207delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.502+18051_502+18052delinsCT MANE Select	ENSP00000279873.7:n.502+18051_502+18052delinsCT
ENST00000644638.1:c.502+18051_502+18052delinsCT	ENSP00000494412.1:n.502+18051_502+18052delinsCT
ENST00000681100.1:c.502+18051_502+18052delinsCT	ENSP00000506119.1:n.502+18051_502+18052delinsCT
ENST00000279873.11:c.502+18051_502+18052delinsCT	ENSP00000279873.7:n.502+18051_502+18052delinsCT
NM_032199.2:c.502+18051_502+18052delinsCT	NP_115575.1:n.502+18051_502+18052delinsCT
XM_011540262.1:c.502+18051_502+18052delinsCT	XP_011538564.1:n.502+18051_502+18052delinsCT
XM_024448230.1:c.-66+18051_-66+18052delinsCT	XP_024303998.1:n.-66+18051_-66+18052delinsCT
NM_032199.3:c.502+18051_502+18052delinsCT MANE Select	NP_115575.1:n.502+18051_502+18052delinsCT