Canonical Allele Identifier: CA593885397

Gene: ARID5B

Linked Data

• dbSNP Id: rs1471973827
• gnomAD v2: 10-63747594-CATGGT-C
• gnomAD v3: 10-61987835-CATGGT-C
• gnomAD v4: 10-61987835-CATGGT-C
• MyVariant Identifiers: chr10:g.63747595_63747599del (hg19) ; chr10:g.61987836_61987840del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61987839_61987843del , CM000672.2:g.61987839_61987843del	GRCh38
NC_000010.10:g.63747598_63747602del , CM000672.1:g.63747598_63747602del	GRCh37
NC_000010.9:g.63417604_63417608del	NCBI36
NG_030027.1:g.91586_91590del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.503-12252_503-12248del MANE Select	ENSP00000279873.7:n.503-12252_503-12248del
ENST00000644638.1:c.503-12252_503-12248del	ENSP00000494412.1:n.503-12252_503-12248del
ENST00000681100.1:c.503-12252_503-12248del	ENSP00000506119.1:n.503-12252_503-12248del
ENST00000279873.11:c.503-12252_503-12248del	ENSP00000279873.7:n.503-12252_503-12248del
NM_032199.2:c.503-12252_503-12248del	NP_115575.1:n.503-12252_503-12248del
XM_011540262.1:c.502+47431_502+47435del	XP_011538564.1:n.502+47431_502+47435del
XM_024448230.1:c.-65-12252_-65-12248del	XP_024303998.1:n.-65-12252_-65-12248del
NM_032199.3:c.503-12252_503-12248del MANE Select	NP_115575.1:n.503-12252_503-12248del