Canonical Allele Identifier: CA366227669

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317156
• MyVariant Identifiers: chr6:g.157502197T>A (hg19) ; chr6:g.157181063T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181063T>A , CM000668.2:g.157181063T>A	GRCh38
NC_000006.11:g.157502197T>A , CM000668.1:g.157502197T>A	GRCh37
NC_000006.10:g.157543889T>A	NCBI36
NG_032093.1:g.408134T>A
NG_032093.2:g.408134T>A
NG_066624.1:g.410038T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3440T>A	ENSP00000055163.8:p.Leu1147His
ENST00000414678.8:c.3509T>A	ENSP00000412835.3:p.Leu1170His
ENST00000637015.2:c.3728T>A	ENSP00000489729.2:p.Leu1243His
ENST00000319584.11:c.1613T>A	ENSP00000313006.7:p.Leu538His
ENST00000346085.10:c.3479T>A	ENSP00000344546.5:p.Leu1160His
ENST00000350026.10:c.3191T>A	ENSP00000055163.7:p.Leu1064His
ENST00000414678.7:c.1757T>A	ENSP00000412835.2:p.Leu586His
ENST00000635849.1:c.920T>A	ENSP00000490948.1:p.Leu307His
ENST00000635957.1:c.554T>A	ENSP00000490385.1:p.Leu185His
ENST00000636930.2:c.3599T>A MANE Select	ENSP00000490491.2:p.Leu1200His
ENST00000636940.1:n.1596T>A
ENST00000637015.1:c.967T>A
ENST00000637568.1:c.881T>A
ENST00000637741.1:n.265T>A
ENST00000637810.1:c.941T>A	ENSP00000489636.1:p.Leu314His
ENST00000637904.1:c.1100T>A	ENSP00000490550.1:p.Leu367His
ENST00000647938.1:c.3230T>A	ENSP00000498155.1:p.Leu1077His
ENST00000319584.10:c.1616T>A	ENSP00000313006.6:p.Leu539His
ENST00000346085.9:c.3230T>A	ENSP00000344546.4:p.Leu1077His
ENST00000350026.9:c.3191T>A	ENSP00000055163.7:p.Leu1064His
ENST00000400790.3:c.392T>A	ENSP00000383596.3:p.Leu131His
ENST00000414678.6:c.1757T>A	ENSP00000412835.2:p.Leu586His
ENST00000478761.3:c.801T>A
NM_017519.2:c.3191T>A	NP_059989.2:p.Leu1064His
NM_020732.3:c.3230T>A	NP_065783.3:p.Leu1077His
XM_005267069.3:c.3350T>A	XP_005267126.2:p.Leu1117His
XM_011535984.1:c.2429T>A	XP_011534286.1:p.Leu810His
XM_011535985.1:c.2249T>A	XP_011534287.1:p.Leu750His
XM_011535986.1:c.2009T>A	XP_011534288.1:p.Leu670His
XM_011535987.1:c.1628T>A	XP_011534289.1:p.Leu543His
XM_011535988.1:c.491T>A	XP_011534290.1:p.Leu164His
NM_001346813.1:c.3350T>A	NP_001333742.1:p.Leu1117His
NM_001363725.1:c.1100T>A	NP_001350654.1:p.Leu367His
XM_011535984.2:c.3560T>A	XP_011534286.2:p.Leu1187His
XM_011535988.3:c.491T>A	XP_011534290.1:p.Leu164His
XM_017011103.2:c.3461T>A	XP_016866592.1:p.Leu1154His
XM_017011104.1:c.3431T>A	XP_016866593.1:p.Leu1144His
XM_017011105.2:c.3401T>A	XP_016866594.1:p.Leu1134His
XM_017011106.2:c.3272T>A	XP_016866595.1:p.Leu1091His
XM_017011107.2:c.3251T>A	XP_016866596.1:p.Leu1084His
XR_002956289.1:n.3643T>A
NM_001363725.2:c.1100T>A	NP_001350654.1:p.Leu367His
NM_001371656.1:c.3479T>A	NP_001358585.1:p.Leu1160His
NM_001374820.1:c.3479T>A	NP_001361749.1:p.Leu1160His
NM_001374828.1:c.3599T>A MANE Select	NP_001361757.1:p.Leu1200His
NM_017519.3:c.3440T>A	NP_059989.3:p.Leu1147His