Canonical Allele Identifier: CA366242906

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376527
• MyVariant Identifiers: chr6:g.157522529C>T (hg19) ; chr6:g.157201395C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201395C>T , CM000668.2:g.157201395C>T	GRCh38
NC_000006.11:g.157522529C>T , CM000668.1:g.157522529C>T	GRCh37
NC_000006.10:g.157564221C>T	NCBI36
NG_032093.1:g.428466C>T
NG_032093.2:g.428466C>T
NG_066624.1:g.430370C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5011C>T	ENSP00000055163.8:p.Pro1671Ser
ENST00000414678.8:c.5080C>T	ENSP00000412835.3:p.Pro1694Ser
ENST00000637015.2:c.5299C>T	ENSP00000489729.2:p.Pro1767Ser
ENST00000346085.10:c.5050C>T	ENSP00000344546.5:p.Pro1684Ser
ENST00000350026.10:c.4762C>T	ENSP00000055163.7:p.Pro1588Ser
ENST00000414678.7:c.3328C>T	ENSP00000412835.2:p.Pro1110Ser
ENST00000635849.1:c.2491C>T	ENSP00000490948.1:p.Pro831Ser
ENST00000635957.1:c.2122C>T	ENSP00000490385.1:p.Pro708Ser
ENST00000636227.1:n.3633C>T
ENST00000636254.1:n.1090C>T
ENST00000636930.2:c.5170C>T MANE Select	ENSP00000490491.2:p.Pro1724Ser
ENST00000636940.1:n.3167C>T
ENST00000637015.1:c.2538C>T
ENST00000637568.1:c.2452C>T
ENST00000637741.1:n.1836C>T
ENST00000637810.1:c.2512C>T	ENSP00000489636.1:p.Pro838Ser
ENST00000637904.1:c.2671C>T	ENSP00000490550.1:p.Pro891Ser
ENST00000647938.1:c.4801C>T	ENSP00000498155.1:p.Pro1601Ser
ENST00000346085.9:c.4801C>T	ENSP00000344546.4:p.Pro1601Ser
ENST00000350026.9:c.4762C>T	ENSP00000055163.7:p.Pro1588Ser
ENST00000414678.6:c.3328C>T	ENSP00000412835.2:p.Pro1110Ser
NM_017519.2:c.4762C>T	NP_059989.2:p.Pro1588Ser
NM_020732.3:c.4801C>T	NP_065783.3:p.Pro1601Ser
XM_005267069.3:c.4921C>T	XP_005267126.2:p.Pro1641Ser
XM_011535984.1:c.4000C>T	XP_011534286.1:p.Pro1334Ser
XM_011535985.1:c.3820C>T	XP_011534287.1:p.Pro1274Ser
XM_011535986.1:c.3580C>T	XP_011534288.1:p.Pro1194Ser
XM_011535987.1:c.3199C>T	XP_011534289.1:p.Pro1067Ser
XM_011535988.1:c.2062C>T	XP_011534290.1:p.Pro688Ser
NM_001346813.1:c.4921C>T	NP_001333742.1:p.Pro1641Ser
NM_001363725.1:c.2671C>T	NP_001350654.1:p.Pro891Ser
XM_011535984.2:c.5131C>T	XP_011534286.2:p.Pro1711Ser
XM_011535988.3:c.2062C>T	XP_011534290.1:p.Pro688Ser
XM_017011103.2:c.5032C>T	XP_016866592.1:p.Pro1678Ser
XM_017011104.1:c.5002C>T	XP_016866593.1:p.Pro1668Ser
XM_017011105.2:c.4972C>T	XP_016866594.1:p.Pro1658Ser
XM_017011106.2:c.4843C>T	XP_016866595.1:p.Pro1615Ser
XM_017011107.2:c.4822C>T	XP_016866596.1:p.Pro1608Ser
XR_002956289.1:n.5117C>T
NM_001363725.2:c.2671C>T	NP_001350654.1:p.Pro891Ser
NM_001371656.1:c.5050C>T	NP_001358585.1:p.Pro1684Ser
NM_001374820.1:c.5050C>T	NP_001361749.1:p.Pro1684Ser
NM_001374828.1:c.5170C>T MANE Select	NP_001361757.1:p.Pro1724Ser
NM_017519.3:c.5011C>T	NP_059989.3:p.Pro1671Ser