Canonical Allele Identifier: CA366389091

Gene: ARID1B

Linked Data

• dbSNP Id: rs1057517704
• gnomAD v2: 6-157469982-C-G
• gnomAD v4: 6-157148848-C-G
• MyVariant Identifiers: chr6:g.157469982C>G (hg19) ; chr6:g.157148848C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148848C>G , CM000668.2:g.157148848C>G	GRCh38
NC_000006.11:g.157469982C>G , CM000668.1:g.157469982C>G	GRCh37
NC_000006.10:g.157511674C>G	NCBI36
NG_032093.1:g.375919C>G
NG_032093.2:g.375919C>G
NG_066624.1:g.377823C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2986C>G	ENSP00000055163.8:p.Gln996Glu
ENST00000414678.8:c.2896C>G	ENSP00000412835.3:p.Gln966Glu
ENST00000637015.2:c.2986C>G	ENSP00000489729.2:p.Gln996Glu
ENST00000319584.11:c.1000C>G	ENSP00000313006.7:p.Gln334Glu
ENST00000346085.10:c.3025C>G	ENSP00000344546.5:p.Gln1009Glu
ENST00000350026.10:c.2737C>G	ENSP00000055163.7:p.Gln913Glu
ENST00000414678.7:c.1144C>G	ENSP00000412835.2:p.Gln382Glu
ENST00000452544.2:n.887C>G
ENST00000635849.1:c.307C>G	ENSP00000490948.1:p.Gln103Glu
ENST00000636426.1:n.120C>G
ENST00000636930.2:c.2986C>G MANE Select	ENSP00000490491.2:p.Gln996Glu
ENST00000637015.1:c.225C>G
ENST00000637568.1:c.29C>G
ENST00000637810.1:c.487C>G	ENSP00000489636.1:p.Gln163Glu
ENST00000637904.1:c.487C>G	ENSP00000490550.1:p.Gln163Glu
ENST00000647938.1:c.2776C>G	ENSP00000498155.1:p.Gln926Glu
ENST00000674190.1:n.1735C>G
ENST00000319584.10:c.1003C>G	ENSP00000313006.6:p.Gln335Glu
ENST00000346085.9:c.2776C>G	ENSP00000344546.4:p.Gln926Glu
ENST00000350026.9:c.2737C>G	ENSP00000055163.7:p.Gln913Glu
ENST00000414678.6:c.1144C>G	ENSP00000412835.2:p.Gln382Glu
ENST00000452544.1:n.833C>G
ENST00000478761.3:c.59C>G
NM_017519.2:c.2737C>G	NP_059989.2:p.Gln913Glu
NM_020732.3:c.2776C>G	NP_065783.3:p.Gln926Glu
XM_005267069.3:c.2737C>G	XP_005267126.2:p.Gln913Glu
XM_011535984.1:c.1687C>G	XP_011534286.1:p.Gln563Glu
XM_011535985.1:c.1507C>G	XP_011534287.1:p.Gln503Glu
XM_011535986.1:c.1267C>G	XP_011534288.1:p.Gln423Glu
XM_011535987.1:c.886C>G	XP_011534289.1:p.Gln296Glu
XM_011535988.1:c.-20+15641C>G	XP_011534290.1:n.-20+15641C>G
NM_001346813.1:c.2737C>G	NP_001333742.1:p.Gln913Glu
NM_001363725.1:c.487C>G	NP_001350654.1:p.Gln163Glu
XM_011535984.2:c.2818C>G	XP_011534286.2:p.Gln940Glu
XM_011535988.3:c.-20+15641C>G	XP_011534290.1:n.-20+15641C>G
XM_017011103.2:c.2818C>G	XP_016866592.1:p.Gln940Glu
XM_017011104.1:c.2818C>G	XP_016866593.1:p.Gln940Glu
XM_017011105.2:c.2818C>G	XP_016866594.1:p.Gln940Glu
XM_017011106.2:c.2818C>G	XP_016866595.1:p.Gln940Glu
XM_017011107.2:c.2638C>G	XP_016866596.1:p.Gln880Glu
XR_002956289.1:n.2901C>G
NM_001363725.2:c.487C>G	NP_001350654.1:p.Gln163Glu
NM_001371656.1:c.3025C>G	NP_001358585.1:p.Gln1009Glu
NM_001374820.1:c.3025C>G	NP_001361749.1:p.Gln1009Glu
NM_001374828.1:c.2986C>G MANE Select	NP_001361757.1:p.Gln996Glu
NM_017519.3:c.2986C>G	NP_059989.3:p.Gln996Glu