Canonical Allele Identifier: CA208313306

Gene: ARID5B

Linked Data

• dbSNP Id: rs750284413
• gnomAD v2: 10-63752165-TG-T
• gnomAD v3: 10-61992406-TG-T
• gnomAD v4: 10-61992406-TG-T
• MyVariant Identifiers: chr10:g.63752166del (hg19) ; chr10:g.61992407del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61992407del , CM000672.2:g.61992407del	GRCh38
NC_000010.10:g.63752166del , CM000672.1:g.63752166del	GRCh37
NC_000010.9:g.63422172del	NCBI36
NG_030027.1:g.96154del

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.503-7684del MANE Select	ENSP00000279873.7:n.503-7684del
ENST00000644638.1:c.503-7684del	ENSP00000494412.1:n.503-7684del
ENST00000681100.1:c.503-7684del	ENSP00000506119.1:n.503-7684del
ENST00000279873.11:c.503-7684del	ENSP00000279873.7:n.503-7684del
NM_032199.2:c.503-7684del	NP_115575.1:n.503-7684del
XM_011540262.1:c.502+51999del	XP_011538564.1:n.502+51999del
XM_024448230.1:c.-65-7684del	XP_024303998.1:n.-65-7684del
NM_032199.3:c.503-7684del MANE Select	NP_115575.1:n.503-7684del