Canonical Allele Identifier: CA929076308

Gene: ARID5B

Linked Data

• dbSNP Id: rs372912200
• gnomAD v3: 10-61992032-C-CAAA
• gnomAD v4: 10-61992032-C-CAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61992043_61992045dup , CM000672.2:g.61992043_61992045dup	GRCh38
NC_000010.10:g.63751802_63751804dup , CM000672.1:g.63751802_63751804dup	GRCh37
NC_000010.9:g.63421808_63421810dup	NCBI36
NG_030027.1:g.95790_95792dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.503-8048_503-8046dup MANE Select	ENSP00000279873.7:n.503-8048_503-8046dup
ENST00000644638.1:c.503-8048_503-8046dup	ENSP00000494412.1:n.503-8048_503-8046dup
ENST00000681100.1:c.503-8048_503-8046dup	ENSP00000506119.1:n.503-8048_503-8046dup
ENST00000279873.11:c.503-8048_503-8046dup	ENSP00000279873.7:n.503-8048_503-8046dup
NM_032199.2:c.503-8048_503-8046dup	NP_115575.1:n.503-8048_503-8046dup
XM_011540262.1:c.502+51635_502+51637dup	XP_011538564.1:n.502+51635_502+51637dup
XM_024448230.1:c.-65-8048_-65-8046dup	XP_024303998.1:n.-65-8048_-65-8046dup
NM_032199.3:c.503-8048_503-8046dup MANE Select	NP_115575.1:n.503-8048_503-8046dup