Canonical Allele Identifier: CA667222829

Gene: ARID5B

Linked Data

• dbSNP Id: rs1466552059
• gnomAD v3: 10-61987994-T-C
• gnomAD v4: 10-61987994-T-C
• MyVariant Identifiers: chr10:g.63747753T>C (hg19) ; chr10:g.61987994T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61987994T>C , CM000672.2:g.61987994T>C	GRCh38
NC_000010.10:g.63747753T>C , CM000672.1:g.63747753T>C	GRCh37
NC_000010.9:g.63417759T>C	NCBI36
NG_030027.1:g.91741T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.503-12097T>C MANE Select	ENSP00000279873.7:n.503-12097T>C
ENST00000644638.1:c.503-12097T>C	ENSP00000494412.1:n.503-12097T>C
ENST00000681100.1:c.503-12097T>C	ENSP00000506119.1:n.503-12097T>C
ENST00000279873.11:c.503-12097T>C	ENSP00000279873.7:n.503-12097T>C
NM_032199.2:c.503-12097T>C	NP_115575.1:n.503-12097T>C
XM_011540262.1:c.502+47586T>C	XP_011538564.1:n.502+47586T>C
XM_024448230.1:c.-65-12097T>C	XP_024303998.1:n.-65-12097T>C
NM_032199.3:c.503-12097T>C MANE Select	NP_115575.1:n.503-12097T>C