Canonical Allele Identifier: CA13192173

Gene: ARID5B

Linked Data

• dbSNP Id: rs7090871
• gnomAD v2: 10-63830286-T-C
• gnomAD v3: 10-62070527-T-C
• gnomAD v4: 10-62070527-T-C
• MyVariant Identifiers: chr10:g.63830286T>C (hg19) ; chr10:g.62070527T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62070527T>C , CM000672.2:g.62070527T>C	GRCh38
NC_000010.10:g.63830286T>C , CM000672.1:g.63830286T>C	GRCh37
NC_000010.9:g.63500292T>C	NCBI36
NG_030027.1:g.174274T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.1199+730T>C MANE Select	ENSP00000279873.7:n.1199+730T>C
ENST00000681100.1:c.1175+730T>C	ENSP00000506119.1:n.1175+730T>C
ENST00000279873.11:c.1199+730T>C	ENSP00000279873.7:n.1199+730T>C
ENST00000309334.5:c.470+730T>C	ENSP00000308862.5:n.470+730T>C
NM_001244638.1:c.470+730T>C	NP_001231567.1:n.470+730T>C
NM_032199.2:c.1199+730T>C	NP_115575.1:n.1199+730T>C
XM_011540262.1:c.968+730T>C	XP_011538564.1:n.968+730T>C
XM_024448230.1:c.632+730T>C	XP_024303998.1:n.632+730T>C
XM_024448231.1:c.-278+730T>C	XP_024303999.1:n.-278+730T>C
NM_032199.3:c.1199+730T>C MANE Select	NP_115575.1:n.1199+730T>C
NM_001244638.2:c.470+730T>C	NP_001231567.1:n.470+730T>C