Canonical Allele Identifier: CA4067034

Gene: ARID1B

Linked Data

• dbSNP Id: rs768277043
• ExAC: 6:157405952 C / G
• gnomAD v2: 6-157405952-C-G
• gnomAD v4: 6-157084818-C-G
• MyVariant Identifiers: chr6:g.157405952C>G (hg19) ; chr6:g.157084818C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084818C>G , CM000668.2:g.157084818C>G	GRCh38
NC_000006.11:g.157405952C>G , CM000668.1:g.157405952C>G	GRCh37
NC_000006.10:g.157447644C>G	NCBI36
NG_032093.1:g.311889C>G
NG_032093.2:g.311889C>G
NG_066624.1:g.313793C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2404C>G	ENSP00000055163.8:p.Pro802Ala
ENST00000414678.8:c.2404C>G	ENSP00000412835.3:p.Pro802Ala
ENST00000637015.2:c.2404C>G	ENSP00000489729.2:p.Pro802Ala
ENST00000319584.11:c.418C>G	ENSP00000313006.7:p.Pro140Ala
ENST00000346085.10:c.2443C>G	ENSP00000344546.5:p.Pro815Ala
ENST00000350026.10:c.2155C>G	ENSP00000055163.7:p.Pro719Ala
ENST00000414678.7:c.652C>G	ENSP00000412835.2:p.Pro218Ala
ENST00000452544.2:n.305C>G
ENST00000493658.2:n.53C>G
ENST00000635849.1:c.-96C>G	ENSP00000490948.1:n.-96C>G
ENST00000636930.2:c.2404C>G MANE Select	ENSP00000490491.2:p.Pro802Ala
ENST00000637003.1:c.-96C>G	ENSP00000489666.1:n.-96C>G
ENST00000637810.1:c.-96C>G	ENSP00000489636.1:n.-96C>G
ENST00000637904.1:c.-96C>G	ENSP00000490550.1:n.-96C>G
ENST00000647938.1:c.2194C>G	ENSP00000498155.1:p.Pro732Ala
ENST00000674190.1:n.1153C>G
ENST00000319584.10:c.421C>G	ENSP00000313006.6:p.Pro141Ala
ENST00000346085.9:c.2194C>G	ENSP00000344546.4:p.Pro732Ala
ENST00000350026.9:c.2155C>G	ENSP00000055163.7:p.Pro719Ala
ENST00000414678.6:c.652C>G	ENSP00000412835.2:p.Pro218Ala
ENST00000452544.1:n.263C>G
ENST00000493658.1:n.53C>G
NM_017519.2:c.2155C>G	NP_059989.2:p.Pro719Ala
NM_020732.3:c.2194C>G	NP_065783.3:p.Pro732Ala
XM_005267069.3:c.2155C>G	XP_005267126.2:p.Pro719Ala
XM_011535984.1:c.1105C>G	XP_011534286.1:p.Pro369Ala
XM_011535985.1:c.1105C>G	XP_011534287.1:p.Pro369Ala
XM_011535986.1:c.685C>G	XP_011534288.1:p.Pro229Ala
XM_011535987.1:c.304C>G	XP_011534289.1:p.Pro102Ala
NM_001346813.1:c.2155C>G	NP_001333742.1:p.Pro719Ala
NM_001363725.1:c.-96C>G	NP_001350654.1:n.-96C>G
XM_011535984.2:c.2236C>G	XP_011534286.2:p.Pro746Ala
XM_017011103.2:c.2236C>G	XP_016866592.1:p.Pro746Ala
XM_017011104.1:c.2236C>G	XP_016866593.1:p.Pro746Ala
XM_017011105.2:c.2236C>G	XP_016866594.1:p.Pro746Ala
XM_017011106.2:c.2236C>G	XP_016866595.1:p.Pro746Ala
XM_017011107.2:c.2236C>G	XP_016866596.1:p.Pro746Ala
XR_002956289.1:n.2319C>G
NM_001363725.2:c.-96C>G	NP_001350654.1:n.-96C>G
NM_001371656.1:c.2443C>G	NP_001358585.1:p.Pro815Ala
NM_001374820.1:c.2443C>G	NP_001361749.1:p.Pro815Ala
NM_001374828.1:c.2404C>G MANE Select	NP_001361757.1:p.Pro802Ala
NM_017519.3:c.2404C>G	NP_059989.3:p.Pro802Ala