Canonical Allele Identifier: CA594019385

Gene: ARID5B

Linked Data

• dbSNP Id: rs1444352734
• gnomAD v2: 10-63721091-T-C
• gnomAD v3: 10-61961332-T-C
• gnomAD v4: 10-61961332-T-C
• MyVariant Identifiers: chr10:g.63721091T>C (hg19) ; chr10:g.61961332T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61961332T>C , CM000672.2:g.61961332T>C	GRCh38
NC_000010.10:g.63721091T>C , CM000672.1:g.63721091T>C	GRCh37
NC_000010.9:g.63391097T>C	NCBI36
NG_030027.1:g.65079T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.502+20924T>C MANE Select	ENSP00000279873.7:n.502+20924T>C
ENST00000644638.1:c.502+20924T>C	ENSP00000494412.1:n.502+20924T>C
ENST00000681100.1:c.502+20924T>C	ENSP00000506119.1:n.502+20924T>C
ENST00000279873.11:c.502+20924T>C	ENSP00000279873.7:n.502+20924T>C
NM_032199.2:c.502+20924T>C	NP_115575.1:n.502+20924T>C
XM_011540262.1:c.502+20924T>C	XP_011538564.1:n.502+20924T>C
XM_024448230.1:c.-66+20924T>C	XP_024303998.1:n.-66+20924T>C
NM_032199.3:c.502+20924T>C MANE Select	NP_115575.1:n.502+20924T>C