Canonical Allele Identifier: CA366242430

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522430T>C (hg19) ; chr6:g.157201296T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201296T>C , CM000668.2:g.157201296T>C	GRCh38
NC_000006.11:g.157522430T>C , CM000668.1:g.157522430T>C	GRCh37
NC_000006.10:g.157564122T>C	NCBI36
NG_032093.1:g.428367T>C
NG_032093.2:g.428367T>C
NG_066624.1:g.430271T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4912T>C	ENSP00000055163.8:p.Ser1638Pro
ENST00000414678.8:c.4981T>C	ENSP00000412835.3:p.Ser1661Pro
ENST00000637015.2:c.5200T>C	ENSP00000489729.2:p.Ser1734Pro
ENST00000346085.10:c.4951T>C	ENSP00000344546.5:p.Ser1651Pro
ENST00000350026.10:c.4663T>C	ENSP00000055163.7:p.Ser1555Pro
ENST00000414678.7:c.3229T>C	ENSP00000412835.2:p.Ser1077Pro
ENST00000635849.1:c.2392T>C	ENSP00000490948.1:p.Ser798Pro
ENST00000635957.1:c.2023T>C	ENSP00000490385.1:p.Ser675Pro
ENST00000636227.1:n.3534T>C
ENST00000636254.1:n.991T>C
ENST00000636930.2:c.5071T>C MANE Select	ENSP00000490491.2:p.Ser1691Pro
ENST00000636940.1:n.3068T>C
ENST00000637015.1:c.2439T>C
ENST00000637568.1:c.2353T>C
ENST00000637741.1:n.1737T>C
ENST00000637810.1:c.2413T>C	ENSP00000489636.1:p.Ser805Pro
ENST00000637904.1:c.2572T>C	ENSP00000490550.1:p.Ser858Pro
ENST00000647938.1:c.4702T>C	ENSP00000498155.1:p.Ser1568Pro
ENST00000346085.9:c.4702T>C	ENSP00000344546.4:p.Ser1568Pro
ENST00000350026.9:c.4663T>C	ENSP00000055163.7:p.Ser1555Pro
ENST00000414678.6:c.3229T>C	ENSP00000412835.2:p.Ser1077Pro
NM_017519.2:c.4663T>C	NP_059989.2:p.Ser1555Pro
NM_020732.3:c.4702T>C	NP_065783.3:p.Ser1568Pro
XM_005267069.3:c.4822T>C	XP_005267126.2:p.Ser1608Pro
XM_011535984.1:c.3901T>C	XP_011534286.1:p.Ser1301Pro
XM_011535985.1:c.3721T>C	XP_011534287.1:p.Ser1241Pro
XM_011535986.1:c.3481T>C	XP_011534288.1:p.Ser1161Pro
XM_011535987.1:c.3100T>C	XP_011534289.1:p.Ser1034Pro
XM_011535988.1:c.1963T>C	XP_011534290.1:p.Ser655Pro
NM_001346813.1:c.4822T>C	NP_001333742.1:p.Ser1608Pro
NM_001363725.1:c.2572T>C	NP_001350654.1:p.Ser858Pro
XM_011535984.2:c.5032T>C	XP_011534286.2:p.Ser1678Pro
XM_011535988.3:c.1963T>C	XP_011534290.1:p.Ser655Pro
XM_017011103.2:c.4933T>C	XP_016866592.1:p.Ser1645Pro
XM_017011104.1:c.4903T>C	XP_016866593.1:p.Ser1635Pro
XM_017011105.2:c.4873T>C	XP_016866594.1:p.Ser1625Pro
XM_017011106.2:c.4744T>C	XP_016866595.1:p.Ser1582Pro
XM_017011107.2:c.4723T>C	XP_016866596.1:p.Ser1575Pro
XR_002956289.1:n.5018T>C
NM_001363725.2:c.2572T>C	NP_001350654.1:p.Ser858Pro
NM_001371656.1:c.4951T>C	NP_001358585.1:p.Ser1651Pro
NM_001374820.1:c.4951T>C	NP_001361749.1:p.Ser1651Pro
NM_001374828.1:c.5071T>C MANE Select	NP_001361757.1:p.Ser1691Pro
NM_017519.3:c.4912T>C	NP_059989.3:p.Ser1638Pro