Canonical Allele Identifier: CA366239838

Gene: ARID1B

Linked Data

• dbSNP Id: rs151115781
• gnomAD v4: 6-157198887-G-T
• MyVariant Identifiers: chr6:g.157520021G>T (hg19) ; chr6:g.157198887G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198887G>T , CM000668.2:g.157198887G>T	GRCh38
NC_000006.11:g.157520021G>T , CM000668.1:g.157520021G>T	GRCh37
NC_000006.10:g.157561713G>T	NCBI36
NG_032093.1:g.425958G>T
NG_032093.2:g.425958G>T
NG_066624.1:g.427862G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4300G>T	ENSP00000055163.8:p.Gly1434Cys
ENST00000414678.8:c.4369G>T	ENSP00000412835.3:p.Gly1457Cys
ENST00000637015.2:c.4588G>T	ENSP00000489729.2:p.Gly1530Cys
ENST00000346085.10:c.4339G>T	ENSP00000344546.5:p.Gly1447Cys
ENST00000350026.10:c.4051G>T	ENSP00000055163.7:p.Gly1351Cys
ENST00000414678.7:c.2617G>T	ENSP00000412835.2:p.Gly873Cys
ENST00000635849.1:c.1780G>T	ENSP00000490948.1:p.Gly594Cys
ENST00000635957.1:c.1411G>T	ENSP00000490385.1:p.Gly471Cys
ENST00000636227.1:n.2922G>T
ENST00000636254.1:n.379G>T
ENST00000636930.2:c.4459G>T MANE Select	ENSP00000490491.2:p.Gly1487Cys
ENST00000636940.1:n.2456G>T
ENST00000637015.1:c.1827G>T
ENST00000637568.1:c.1741G>T
ENST00000637741.1:n.1125G>T
ENST00000637810.1:c.1801G>T	ENSP00000489636.1:p.Gly601Cys
ENST00000637904.1:c.1960G>T	ENSP00000490550.1:p.Gly654Cys
ENST00000647938.1:c.4090G>T	ENSP00000498155.1:p.Gly1364Cys
ENST00000346085.9:c.4090G>T	ENSP00000344546.4:p.Gly1364Cys
ENST00000350026.9:c.4051G>T	ENSP00000055163.7:p.Gly1351Cys
ENST00000414678.6:c.2617G>T	ENSP00000412835.2:p.Gly873Cys
NM_017519.2:c.4051G>T	NP_059989.2:p.Gly1351Cys
NM_020732.3:c.4090G>T	NP_065783.3:p.Gly1364Cys
XM_005267069.3:c.4210G>T	XP_005267126.2:p.Gly1404Cys
XM_011535984.1:c.3289G>T	XP_011534286.1:p.Gly1097Cys
XM_011535985.1:c.3109G>T	XP_011534287.1:p.Gly1037Cys
XM_011535986.1:c.2869G>T	XP_011534288.1:p.Gly957Cys
XM_011535987.1:c.2488G>T	XP_011534289.1:p.Gly830Cys
XM_011535988.1:c.1351G>T	XP_011534290.1:p.Gly451Cys
NM_001346813.1:c.4210G>T	NP_001333742.1:p.Gly1404Cys
NM_001363725.1:c.1960G>T	NP_001350654.1:p.Gly654Cys
XM_011535984.2:c.4420G>T	XP_011534286.2:p.Gly1474Cys
XM_011535988.3:c.1351G>T	XP_011534290.1:p.Gly451Cys
XM_017011103.2:c.4321G>T	XP_016866592.1:p.Gly1441Cys
XM_017011104.1:c.4291G>T	XP_016866593.1:p.Gly1431Cys
XM_017011105.2:c.4261G>T	XP_016866594.1:p.Gly1421Cys
XM_017011106.2:c.4132G>T	XP_016866595.1:p.Gly1378Cys
XM_017011107.2:c.4111G>T	XP_016866596.1:p.Gly1371Cys
XR_002956289.1:n.4427-1818G>T
NM_001363725.2:c.1960G>T	NP_001350654.1:p.Gly654Cys
NM_001371656.1:c.4339G>T	NP_001358585.1:p.Gly1447Cys
NM_001374820.1:c.4339G>T	NP_001361749.1:p.Gly1447Cys
NM_001374828.1:c.4459G>T MANE Select	NP_001361757.1:p.Gly1487Cys
NM_017519.3:c.4300G>T	NP_059989.3:p.Gly1434Cys