Canonical Allele Identifier: CA366241657

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201039-G-T
• MyVariant Identifiers: chr6:g.157522173G>T (hg19) ; chr6:g.157201039G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201039G>T , CM000668.2:g.157201039G>T	GRCh38
NC_000006.11:g.157522173G>T , CM000668.1:g.157522173G>T	GRCh37
NC_000006.10:g.157563865G>T	NCBI36
NG_032093.1:g.428110G>T
NG_032093.2:g.428110G>T
NG_066624.1:g.430014G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4655G>T	ENSP00000055163.8:p.Gly1552Val
ENST00000414678.8:c.4724G>T	ENSP00000412835.3:p.Gly1575Val
ENST00000637015.2:c.4943G>T	ENSP00000489729.2:p.Gly1648Val
ENST00000346085.10:c.4694G>T	ENSP00000344546.5:p.Gly1565Val
ENST00000350026.10:c.4406G>T	ENSP00000055163.7:p.Gly1469Val
ENST00000414678.7:c.2972G>T	ENSP00000412835.2:p.Gly991Val
ENST00000635849.1:c.2135G>T	ENSP00000490948.1:p.Gly712Val
ENST00000635957.1:c.1766G>T	ENSP00000490385.1:p.Gly589Val
ENST00000636227.1:n.3277G>T
ENST00000636254.1:n.734G>T
ENST00000636930.2:c.4814G>T MANE Select	ENSP00000490491.2:p.Gly1605Val
ENST00000636940.1:n.2811G>T
ENST00000637015.1:c.2182G>T
ENST00000637568.1:c.2096G>T
ENST00000637741.1:n.1480G>T
ENST00000637810.1:c.2156G>T	ENSP00000489636.1:p.Gly719Val
ENST00000637904.1:c.2315G>T	ENSP00000490550.1:p.Gly772Val
ENST00000647938.1:c.4445G>T	ENSP00000498155.1:p.Gly1482Val
ENST00000346085.9:c.4445G>T	ENSP00000344546.4:p.Gly1482Val
ENST00000350026.9:c.4406G>T	ENSP00000055163.7:p.Gly1469Val
ENST00000414678.6:c.2972G>T	ENSP00000412835.2:p.Gly991Val
NM_017519.2:c.4406G>T	NP_059989.2:p.Gly1469Val
NM_020732.3:c.4445G>T	NP_065783.3:p.Gly1482Val
XM_005267069.3:c.4565G>T	XP_005267126.2:p.Gly1522Val
XM_011535984.1:c.3644G>T	XP_011534286.1:p.Gly1215Val
XM_011535985.1:c.3464G>T	XP_011534287.1:p.Gly1155Val
XM_011535986.1:c.3224G>T	XP_011534288.1:p.Gly1075Val
XM_011535987.1:c.2843G>T	XP_011534289.1:p.Gly948Val
XM_011535988.1:c.1706G>T	XP_011534290.1:p.Gly569Val
NM_001346813.1:c.4565G>T	NP_001333742.1:p.Gly1522Val
NM_001363725.1:c.2315G>T	NP_001350654.1:p.Gly772Val
XM_011535984.2:c.4775G>T	XP_011534286.2:p.Gly1592Val
XM_011535988.3:c.1706G>T	XP_011534290.1:p.Gly569Val
XM_017011103.2:c.4676G>T	XP_016866592.1:p.Gly1559Val
XM_017011104.1:c.4646G>T	XP_016866593.1:p.Gly1549Val
XM_017011105.2:c.4616G>T	XP_016866594.1:p.Gly1539Val
XM_017011106.2:c.4487G>T	XP_016866595.1:p.Gly1496Val
XM_017011107.2:c.4466G>T	XP_016866596.1:p.Gly1489Val
XR_002956289.1:n.4761G>T
NM_001363725.2:c.2315G>T	NP_001350654.1:p.Gly772Val
NM_001371656.1:c.4694G>T	NP_001358585.1:p.Gly1565Val
NM_001374820.1:c.4694G>T	NP_001361749.1:p.Gly1565Val
NM_001374828.1:c.4814G>T MANE Select	NP_001361757.1:p.Gly1605Val
NM_017519.3:c.4655G>T	NP_059989.3:p.Gly1552Val