Canonical Allele Identifier: CA366228224

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317594
• MyVariant Identifiers: chr6:g.157502265C>A (hg19) ; chr6:g.157181131C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181131C>A , CM000668.2:g.157181131C>A	GRCh38
NC_000006.11:g.157502265C>A , CM000668.1:g.157502265C>A	GRCh37
NC_000006.10:g.157543957C>A	NCBI36
NG_032093.1:g.408202C>A
NG_032093.2:g.408202C>A
NG_066624.1:g.410106C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3508C>A	ENSP00000055163.8:p.Leu1170Met
ENST00000414678.8:c.3577C>A	ENSP00000412835.3:p.Leu1193Met
ENST00000637015.2:c.3796C>A	ENSP00000489729.2:p.Leu1266Met
ENST00000319584.11:c.1681C>A	ENSP00000313006.7:p.Leu561Met
ENST00000346085.10:c.3547C>A	ENSP00000344546.5:p.Leu1183Met
ENST00000350026.10:c.3259C>A	ENSP00000055163.7:p.Leu1087Met
ENST00000414678.7:c.1825C>A	ENSP00000412835.2:p.Leu609Met
ENST00000635849.1:c.988C>A	ENSP00000490948.1:p.Leu330Met
ENST00000635957.1:c.622C>A	ENSP00000490385.1:p.Leu208Met
ENST00000636930.2:c.3667C>A MANE Select	ENSP00000490491.2:p.Leu1223Met
ENST00000636940.1:n.1664C>A
ENST00000637015.1:c.1035C>A
ENST00000637568.1:c.949C>A
ENST00000637741.1:n.333C>A
ENST00000637810.1:c.1009C>A	ENSP00000489636.1:p.Leu337Met
ENST00000637904.1:c.1168C>A	ENSP00000490550.1:p.Leu390Met
ENST00000647938.1:c.3298C>A	ENSP00000498155.1:p.Leu1100Met
ENST00000319584.10:c.1684C>A	ENSP00000313006.6:p.Leu562Met
ENST00000346085.9:c.3298C>A	ENSP00000344546.4:p.Leu1100Met
ENST00000350026.9:c.3259C>A	ENSP00000055163.7:p.Leu1087Met
ENST00000400790.3:c.460C>A	ENSP00000383596.3:p.Leu154Met
ENST00000414678.6:c.1825C>A	ENSP00000412835.2:p.Leu609Met
ENST00000478761.3:c.869C>A
NM_017519.2:c.3259C>A	NP_059989.2:p.Leu1087Met
NM_020732.3:c.3298C>A	NP_065783.3:p.Leu1100Met
XM_005267069.3:c.3418C>A	XP_005267126.2:p.Leu1140Met
XM_011535984.1:c.2497C>A	XP_011534286.1:p.Leu833Met
XM_011535985.1:c.2317C>A	XP_011534287.1:p.Leu773Met
XM_011535986.1:c.2077C>A	XP_011534288.1:p.Leu693Met
XM_011535987.1:c.1696C>A	XP_011534289.1:p.Leu566Met
XM_011535988.1:c.559C>A	XP_011534290.1:p.Leu187Met
NM_001346813.1:c.3418C>A	NP_001333742.1:p.Leu1140Met
NM_001363725.1:c.1168C>A	NP_001350654.1:p.Leu390Met
XM_011535984.2:c.3628C>A	XP_011534286.2:p.Leu1210Met
XM_011535988.3:c.559C>A	XP_011534290.1:p.Leu187Met
XM_017011103.2:c.3529C>A	XP_016866592.1:p.Leu1177Met
XM_017011104.1:c.3499C>A	XP_016866593.1:p.Leu1167Met
XM_017011105.2:c.3469C>A	XP_016866594.1:p.Leu1157Met
XM_017011106.2:c.3340C>A	XP_016866595.1:p.Leu1114Met
XM_017011107.2:c.3319C>A	XP_016866596.1:p.Leu1107Met
XR_002956289.1:n.3711C>A
NM_001363725.2:c.1168C>A	NP_001350654.1:p.Leu390Met
NM_001371656.1:c.3547C>A	NP_001358585.1:p.Leu1183Met
NM_001374820.1:c.3547C>A	NP_001361749.1:p.Leu1183Met
NM_001374828.1:c.3667C>A MANE Select	NP_001361757.1:p.Leu1223Met
NM_017519.3:c.3508C>A	NP_059989.3:p.Leu1170Met