Canonical Allele Identifier: CA366242669

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522480G>T (hg19) ; chr6:g.157201346G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201346G>T , CM000668.2:g.157201346G>T	GRCh38
NC_000006.11:g.157522480G>T , CM000668.1:g.157522480G>T	GRCh37
NC_000006.10:g.157564172G>T	NCBI36
NG_032093.1:g.428417G>T
NG_032093.2:g.428417G>T
NG_066624.1:g.430321G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4962G>T	ENSP00000055163.8:p.Met1654Ile
ENST00000414678.8:c.5031G>T	ENSP00000412835.3:p.Met1677Ile
ENST00000637015.2:c.5250G>T	ENSP00000489729.2:p.Met1750Ile
ENST00000346085.10:c.5001G>T	ENSP00000344546.5:p.Met1667Ile
ENST00000350026.10:c.4713G>T	ENSP00000055163.7:p.Met1571Ile
ENST00000414678.7:c.3279G>T	ENSP00000412835.2:p.Met1093Ile
ENST00000635849.1:c.2442G>T	ENSP00000490948.1:p.Met814Ile
ENST00000635957.1:c.2073G>T	ENSP00000490385.1:p.Met691Ile
ENST00000636227.1:n.3584G>T
ENST00000636254.1:n.1041G>T
ENST00000636930.2:c.5121G>T MANE Select	ENSP00000490491.2:p.Met1707Ile
ENST00000636940.1:n.3118G>T
ENST00000637015.1:c.2489G>T
ENST00000637568.1:c.2403G>T
ENST00000637741.1:n.1787G>T
ENST00000637810.1:c.2463G>T	ENSP00000489636.1:p.Met821Ile
ENST00000637904.1:c.2622G>T	ENSP00000490550.1:p.Met874Ile
ENST00000647938.1:c.4752G>T	ENSP00000498155.1:p.Met1584Ile
ENST00000346085.9:c.4752G>T	ENSP00000344546.4:p.Met1584Ile
ENST00000350026.9:c.4713G>T	ENSP00000055163.7:p.Met1571Ile
ENST00000414678.6:c.3279G>T	ENSP00000412835.2:p.Met1093Ile
NM_017519.2:c.4713G>T	NP_059989.2:p.Met1571Ile
NM_020732.3:c.4752G>T	NP_065783.3:p.Met1584Ile
XM_005267069.3:c.4872G>T	XP_005267126.2:p.Met1624Ile
XM_011535984.1:c.3951G>T	XP_011534286.1:p.Met1317Ile
XM_011535985.1:c.3771G>T	XP_011534287.1:p.Met1257Ile
XM_011535986.1:c.3531G>T	XP_011534288.1:p.Met1177Ile
XM_011535987.1:c.3150G>T	XP_011534289.1:p.Met1050Ile
XM_011535988.1:c.2013G>T	XP_011534290.1:p.Met671Ile
NM_001346813.1:c.4872G>T	NP_001333742.1:p.Met1624Ile
NM_001363725.1:c.2622G>T	NP_001350654.1:p.Met874Ile
XM_011535984.2:c.5082G>T	XP_011534286.2:p.Met1694Ile
XM_011535988.3:c.2013G>T	XP_011534290.1:p.Met671Ile
XM_017011103.2:c.4983G>T	XP_016866592.1:p.Met1661Ile
XM_017011104.1:c.4953G>T	XP_016866593.1:p.Met1651Ile
XM_017011105.2:c.4923G>T	XP_016866594.1:p.Met1641Ile
XM_017011106.2:c.4794G>T	XP_016866595.1:p.Met1598Ile
XM_017011107.2:c.4773G>T	XP_016866596.1:p.Met1591Ile
XR_002956289.1:n.5068G>T
NM_001363725.2:c.2622G>T	NP_001350654.1:p.Met874Ile
NM_001371656.1:c.5001G>T	NP_001358585.1:p.Met1667Ile
NM_001374820.1:c.5001G>T	NP_001361749.1:p.Met1667Ile
NM_001374828.1:c.5121G>T MANE Select	NP_001361757.1:p.Met1707Ile
NM_017519.3:c.4962G>T	NP_059989.3:p.Met1654Ile