Canonical Allele Identifier: CA667222825

Gene: ARID5B

Linked Data

• dbSNP Id: rs1333800189
• gnomAD v3: 10-61987990-G-A
• gnomAD v4: 10-61987990-G-A
• MyVariant Identifiers: chr10:g.63747749G>A (hg19) ; chr10:g.61987990G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61987990G>A , CM000672.2:g.61987990G>A	GRCh38
NC_000010.10:g.63747749G>A , CM000672.1:g.63747749G>A	GRCh37
NC_000010.9:g.63417755G>A	NCBI36
NG_030027.1:g.91737G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.503-12101G>A MANE Select	ENSP00000279873.7:n.503-12101G>A
ENST00000644638.1:c.503-12101G>A	ENSP00000494412.1:n.503-12101G>A
ENST00000681100.1:c.503-12101G>A	ENSP00000506119.1:n.503-12101G>A
ENST00000279873.11:c.503-12101G>A	ENSP00000279873.7:n.503-12101G>A
NM_032199.2:c.503-12101G>A	NP_115575.1:n.503-12101G>A
XM_011540262.1:c.502+47582G>A	XP_011538564.1:n.502+47582G>A
XM_024448230.1:c.-65-12101G>A	XP_024303998.1:n.-65-12101G>A
NM_032199.3:c.503-12101G>A MANE Select	NP_115575.1:n.503-12101G>A