Canonical Allele Identifier: CA366228027

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317335
• MyVariant Identifiers: chr6:g.157502227T>G (hg19) ; chr6:g.157181093T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181093T>G , CM000668.2:g.157181093T>G	GRCh38
NC_000006.11:g.157502227T>G , CM000668.1:g.157502227T>G	GRCh37
NC_000006.10:g.157543919T>G	NCBI36
NG_032093.1:g.408164T>G
NG_032093.2:g.408164T>G
NG_066624.1:g.410068T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3470T>G	ENSP00000055163.8:p.Val1157Gly
ENST00000414678.8:c.3539T>G	ENSP00000412835.3:p.Val1180Gly
ENST00000637015.2:c.3758T>G	ENSP00000489729.2:p.Val1253Gly
ENST00000319584.11:c.1643T>G	ENSP00000313006.7:p.Val548Gly
ENST00000346085.10:c.3509T>G	ENSP00000344546.5:p.Val1170Gly
ENST00000350026.10:c.3221T>G	ENSP00000055163.7:p.Val1074Gly
ENST00000414678.7:c.1787T>G	ENSP00000412835.2:p.Val596Gly
ENST00000635849.1:c.950T>G	ENSP00000490948.1:p.Val317Gly
ENST00000635957.1:c.584T>G	ENSP00000490385.1:p.Val195Gly
ENST00000636930.2:c.3629T>G MANE Select	ENSP00000490491.2:p.Val1210Gly
ENST00000636940.1:n.1626T>G
ENST00000637015.1:c.997T>G
ENST00000637568.1:c.911T>G
ENST00000637741.1:n.295T>G
ENST00000637810.1:c.971T>G	ENSP00000489636.1:p.Val324Gly
ENST00000637904.1:c.1130T>G	ENSP00000490550.1:p.Val377Gly
ENST00000647938.1:c.3260T>G	ENSP00000498155.1:p.Val1087Gly
ENST00000319584.10:c.1646T>G	ENSP00000313006.6:p.Val549Gly
ENST00000346085.9:c.3260T>G	ENSP00000344546.4:p.Val1087Gly
ENST00000350026.9:c.3221T>G	ENSP00000055163.7:p.Val1074Gly
ENST00000400790.3:c.422T>G	ENSP00000383596.3:p.Val141Gly
ENST00000414678.6:c.1787T>G	ENSP00000412835.2:p.Val596Gly
ENST00000478761.3:c.831T>G
NM_017519.2:c.3221T>G	NP_059989.2:p.Val1074Gly
NM_020732.3:c.3260T>G	NP_065783.3:p.Val1087Gly
XM_005267069.3:c.3380T>G	XP_005267126.2:p.Val1127Gly
XM_011535984.1:c.2459T>G	XP_011534286.1:p.Val820Gly
XM_011535985.1:c.2279T>G	XP_011534287.1:p.Val760Gly
XM_011535986.1:c.2039T>G	XP_011534288.1:p.Val680Gly
XM_011535987.1:c.1658T>G	XP_011534289.1:p.Val553Gly
XM_011535988.1:c.521T>G	XP_011534290.1:p.Val174Gly
NM_001346813.1:c.3380T>G	NP_001333742.1:p.Val1127Gly
NM_001363725.1:c.1130T>G	NP_001350654.1:p.Val377Gly
XM_011535984.2:c.3590T>G	XP_011534286.2:p.Val1197Gly
XM_011535988.3:c.521T>G	XP_011534290.1:p.Val174Gly
XM_017011103.2:c.3491T>G	XP_016866592.1:p.Val1164Gly
XM_017011104.1:c.3461T>G	XP_016866593.1:p.Val1154Gly
XM_017011105.2:c.3431T>G	XP_016866594.1:p.Val1144Gly
XM_017011106.2:c.3302T>G	XP_016866595.1:p.Val1101Gly
XM_017011107.2:c.3281T>G	XP_016866596.1:p.Val1094Gly
XR_002956289.1:n.3673T>G
NM_001363725.2:c.1130T>G	NP_001350654.1:p.Val377Gly
NM_001371656.1:c.3509T>G	NP_001358585.1:p.Val1170Gly
NM_001374820.1:c.3509T>G	NP_001361749.1:p.Val1170Gly
NM_001374828.1:c.3629T>G MANE Select	NP_001361757.1:p.Val1210Gly
NM_017519.3:c.3470T>G	NP_059989.3:p.Val1157Gly