Canonical Allele Identifier: CA667209226

Gene: ARID5B

Linked Data

• dbSNP Id: rs1274245236
• gnomAD v3: 10-61958660-CTT-C
• gnomAD v4: 10-61958660-CTT-C
• MyVariant Identifiers: chr10:g.63718420_63718421del (hg19) ; chr10:g.61958661_61958662del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61958661_61958662del , CM000672.2:g.61958661_61958662del	GRCh38
NC_000010.10:g.63718420_63718421del , CM000672.1:g.63718420_63718421del	GRCh37
NC_000010.9:g.63388426_63388427del	NCBI36
NG_030027.1:g.62408_62409del

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.502+18253_502+18254del MANE Select	ENSP00000279873.7:n.502+18253_502+18254del
ENST00000644638.1:c.502+18253_502+18254del	ENSP00000494412.1:n.502+18253_502+18254del
ENST00000681100.1:c.502+18253_502+18254del	ENSP00000506119.1:n.502+18253_502+18254del
ENST00000279873.11:c.502+18253_502+18254del	ENSP00000279873.7:n.502+18253_502+18254del
NM_032199.2:c.502+18253_502+18254del	NP_115575.1:n.502+18253_502+18254del
XM_011540262.1:c.502+18253_502+18254del	XP_011538564.1:n.502+18253_502+18254del
XM_024448230.1:c.-66+18253_-66+18254del	XP_024303998.1:n.-66+18253_-66+18254del
NM_032199.3:c.502+18253_502+18254del MANE Select	NP_115575.1:n.502+18253_502+18254del