Canonical Allele Identifier: CA929076397

Gene: ARID5B

Linked Data

• dbSNP Id: rs1838937411

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61992296_61992297del , CM000672.2:g.61992296_61992297del	GRCh38
NC_000010.10:g.63752055_63752056del , CM000672.1:g.63752055_63752056del	GRCh37
NC_000010.9:g.63422061_63422062del	NCBI36
NG_030027.1:g.96043_96044del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.503-7795_503-7794del MANE Select	ENSP00000279873.7:n.503-7795_503-7794del
ENST00000644638.1:c.503-7795_503-7794del	ENSP00000494412.1:n.503-7795_503-7794del
ENST00000681100.1:c.503-7795_503-7794del	ENSP00000506119.1:n.503-7795_503-7794del
ENST00000279873.11:c.503-7795_503-7794del	ENSP00000279873.7:n.503-7795_503-7794del
NM_032199.2:c.503-7795_503-7794del	NP_115575.1:n.503-7795_503-7794del
XM_011540262.1:c.502+51888_502+51889del	XP_011538564.1:n.502+51888_502+51889del
XM_024448230.1:c.-65-7795_-65-7794del	XP_024303998.1:n.-65-7795_-65-7794del
NM_032199.3:c.503-7795_503-7794del MANE Select	NP_115575.1:n.503-7795_503-7794del