Canonical Allele Identifier: CA452978308

Gene: ARID1B

Linked Data

• gnomAD v2: 6-157522441-G-A
• gnomAD v4: 6-157201307-G-A
• MyVariant Identifiers: chr6:g.157522441G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201307G>A , CM000668.2:g.157201307G>A	GRCh38
NC_000006.11:g.157522441G>A , CM000668.1:g.157522441G>A	GRCh37
NC_000006.10:g.157564133G>A	NCBI36
NG_032093.1:g.428378G>A
NG_032093.2:g.428378G>A
NG_066624.1:g.430282G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4923G>A	ENSP00000055163.8:p.Lys1641=
ENST00000414678.8:c.4992G>A	ENSP00000412835.3:p.Lys1664=
ENST00000637015.2:c.5211G>A	ENSP00000489729.2:p.Lys1737=
ENST00000346085.10:c.4962G>A	ENSP00000344546.5:p.Lys1654=
ENST00000350026.10:c.4674G>A	ENSP00000055163.7:p.Lys1558=
ENST00000414678.7:c.3240G>A	ENSP00000412835.2:p.Lys1080=
ENST00000635849.1:c.2403G>A	ENSP00000490948.1:p.Lys801=
ENST00000635957.1:c.2034G>A	ENSP00000490385.1:p.Lys678=
ENST00000636227.1:n.3545G>A
ENST00000636254.1:n.1002G>A
ENST00000636930.2:c.5082G>A MANE Select	ENSP00000490491.2:p.Lys1694=
ENST00000636940.1:n.3079G>A
ENST00000637015.1:c.2450G>A
ENST00000637568.1:c.2364G>A
ENST00000637741.1:n.1748G>A
ENST00000637810.1:c.2424G>A	ENSP00000489636.1:p.Lys808=
ENST00000637904.1:c.2583G>A	ENSP00000490550.1:p.Lys861=
ENST00000647938.1:c.4713G>A	ENSP00000498155.1:p.Lys1571=
ENST00000346085.9:c.4713G>A	ENSP00000344546.4:p.Lys1571=
ENST00000350026.9:c.4674G>A	ENSP00000055163.7:p.Lys1558=
ENST00000414678.6:c.3240G>A	ENSP00000412835.2:p.Lys1080=
NM_017519.2:c.4674G>A	NP_059989.2:p.Lys1558=
NM_020732.3:c.4713G>A	NP_065783.3:p.Lys1571=
XM_005267069.3:c.4833G>A	XP_005267126.2:p.Lys1611=
XM_011535984.1:c.3912G>A	XP_011534286.1:p.Lys1304=
XM_011535985.1:c.3732G>A	XP_011534287.1:p.Lys1244=
XM_011535986.1:c.3492G>A	XP_011534288.1:p.Lys1164=
XM_011535987.1:c.3111G>A	XP_011534289.1:p.Lys1037=
XM_011535988.1:c.1974G>A	XP_011534290.1:p.Lys658=
NM_001346813.1:c.4833G>A	NP_001333742.1:p.Lys1611=
NM_001363725.1:c.2583G>A	NP_001350654.1:p.Lys861=
XM_011535984.2:c.5043G>A	XP_011534286.2:p.Lys1681=
XM_011535988.3:c.1974G>A	XP_011534290.1:p.Lys658=
XM_017011103.2:c.4944G>A	XP_016866592.1:p.Lys1648=
XM_017011104.1:c.4914G>A	XP_016866593.1:p.Lys1638=
XM_017011105.2:c.4884G>A	XP_016866594.1:p.Lys1628=
XM_017011106.2:c.4755G>A	XP_016866595.1:p.Lys1585=
XM_017011107.2:c.4734G>A	XP_016866596.1:p.Lys1578=
XR_002956289.1:n.5029G>A
NM_001363725.2:c.2583G>A	NP_001350654.1:p.Lys861=
NM_001371656.1:c.4962G>A	NP_001358585.1:p.Lys1654=
NM_001374820.1:c.4962G>A	NP_001361749.1:p.Lys1654=
NM_001374828.1:c.5082G>A MANE Select	NP_001361757.1:p.Lys1694=
NM_017519.3:c.4923G>A	NP_059989.3:p.Lys1641=