Canonical Allele Identifier: CA150846254

Gene: ARID1B

Linked Data

• dbSNP Id: rs1002364077
• MyVariant Identifiers: chr6:g.157469994G>A (hg19) ; chr6:g.157148860G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148860G>A , CM000668.2:g.157148860G>A	GRCh38
NC_000006.11:g.157469994G>A , CM000668.1:g.157469994G>A	GRCh37
NC_000006.10:g.157511686G>A	NCBI36
NG_032093.1:g.375931G>A
NG_032093.2:g.375931G>A
NG_066624.1:g.377835G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.2998G>A	ENSP00000055163.8:p.Gly1000Arg
ENST00000414678.8:c.2908G>A	ENSP00000412835.3:p.Gly970Arg
ENST00000637015.2:c.2998G>A	ENSP00000489729.2:p.Gly1000Arg
ENST00000319584.11:c.1012G>A	ENSP00000313006.7:p.Gly338Arg
ENST00000346085.10:c.3037G>A	ENSP00000344546.5:p.Gly1013Arg
ENST00000350026.10:c.2749G>A	ENSP00000055163.7:p.Gly917Arg
ENST00000414678.7:c.1156G>A	ENSP00000412835.2:p.Gly386Arg
ENST00000452544.2:n.899G>A
ENST00000635849.1:c.319G>A	ENSP00000490948.1:p.Gly107Arg
ENST00000636426.1:n.132G>A
ENST00000636930.2:c.2998G>A MANE Select	ENSP00000490491.2:p.Gly1000Arg
ENST00000637015.1:c.237G>A
ENST00000637568.1:c.41G>A
ENST00000637810.1:c.499G>A	ENSP00000489636.1:p.Gly167Arg
ENST00000637904.1:c.499G>A	ENSP00000490550.1:p.Gly167Arg
ENST00000647938.1:c.2788G>A	ENSP00000498155.1:p.Gly930Arg
ENST00000674190.1:n.1747G>A
ENST00000319584.10:c.1015G>A	ENSP00000313006.6:p.Gly339Arg
ENST00000346085.9:c.2788G>A	ENSP00000344546.4:p.Gly930Arg
ENST00000350026.9:c.2749G>A	ENSP00000055163.7:p.Gly917Arg
ENST00000414678.6:c.1156G>A	ENSP00000412835.2:p.Gly386Arg
ENST00000452544.1:n.845G>A
ENST00000478761.3:c.71G>A
NM_017519.2:c.2749G>A	NP_059989.2:p.Gly917Arg
NM_020732.3:c.2788G>A	NP_065783.3:p.Gly930Arg
XM_005267069.3:c.2749G>A	XP_005267126.2:p.Gly917Arg
XM_011535984.1:c.1699G>A	XP_011534286.1:p.Gly567Arg
XM_011535985.1:c.1519G>A	XP_011534287.1:p.Gly507Arg
XM_011535986.1:c.1279G>A	XP_011534288.1:p.Gly427Arg
XM_011535987.1:c.898G>A	XP_011534289.1:p.Gly300Arg
XM_011535988.1:c.-20+15653G>A	XP_011534290.1:n.-20+15653G>A
NM_001346813.1:c.2749G>A	NP_001333742.1:p.Gly917Arg
NM_001363725.1:c.499G>A	NP_001350654.1:p.Gly167Arg
XM_011535984.2:c.2830G>A	XP_011534286.2:p.Gly944Arg
XM_011535988.3:c.-20+15653G>A	XP_011534290.1:n.-20+15653G>A
XM_017011103.2:c.2830G>A	XP_016866592.1:p.Gly944Arg
XM_017011104.1:c.2830G>A	XP_016866593.1:p.Gly944Arg
XM_017011105.2:c.2830G>A	XP_016866594.1:p.Gly944Arg
XM_017011106.2:c.2830G>A	XP_016866595.1:p.Gly944Arg
XM_017011107.2:c.2650G>A	XP_016866596.1:p.Gly884Arg
XR_002956289.1:n.2913G>A
NM_001363725.2:c.499G>A	NP_001350654.1:p.Gly167Arg
NM_001371656.1:c.3037G>A	NP_001358585.1:p.Gly1013Arg
NM_001374820.1:c.3037G>A	NP_001361749.1:p.Gly1013Arg
NM_001374828.1:c.2998G>A MANE Select	NP_001361757.1:p.Gly1000Arg
NM_017519.3:c.2998G>A	NP_059989.3:p.Gly1000Arg