Canonical Allele Identifier: CA366234757

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511189T>A (hg19) ; chr6:g.157190055T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190055T>A , CM000668.2:g.157190055T>A	GRCh38
NC_000006.11:g.157511189T>A , CM000668.1:g.157511189T>A	GRCh37
NC_000006.10:g.157552881T>A	NCBI36
NG_032093.1:g.417126T>A
NG_032093.2:g.417126T>A
NG_066624.1:g.419030T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3917T>A	ENSP00000055163.8:p.Val1306Glu
ENST00000414678.8:c.3986T>A	ENSP00000412835.3:p.Val1329Glu
ENST00000637015.2:c.4205T>A	ENSP00000489729.2:p.Val1402Glu
ENST00000346085.10:c.3956T>A	ENSP00000344546.5:p.Val1319Glu
ENST00000350026.10:c.3668T>A	ENSP00000055163.7:p.Val1223Glu
ENST00000414678.7:c.2234T>A	ENSP00000412835.2:p.Val745Glu
ENST00000635849.1:c.1397T>A	ENSP00000490948.1:p.Val466Glu
ENST00000635957.1:c.1028T>A	ENSP00000490385.1:p.Val343Glu
ENST00000636930.2:c.4076T>A MANE Select	ENSP00000490491.2:p.Val1359Glu
ENST00000636940.1:n.2073T>A
ENST00000637015.1:c.1444T>A
ENST00000637568.1:c.1358T>A
ENST00000637741.1:n.742T>A
ENST00000637810.1:c.1418T>A	ENSP00000489636.1:p.Val473Glu
ENST00000637904.1:c.1577T>A	ENSP00000490550.1:p.Val526Glu
ENST00000647938.1:c.3707T>A	ENSP00000498155.1:p.Val1236Glu
ENST00000346085.9:c.3707T>A	ENSP00000344546.4:p.Val1236Glu
ENST00000350026.9:c.3668T>A	ENSP00000055163.7:p.Val1223Glu
ENST00000414678.6:c.2234T>A	ENSP00000412835.2:p.Val745Glu
NM_017519.2:c.3668T>A	NP_059989.2:p.Val1223Glu
NM_020732.3:c.3707T>A	NP_065783.3:p.Val1236Glu
XM_005267069.3:c.3827T>A	XP_005267126.2:p.Val1276Glu
XM_011535984.1:c.2906T>A	XP_011534286.1:p.Val969Glu
XM_011535985.1:c.2726T>A	XP_011534287.1:p.Val909Glu
XM_011535986.1:c.2486T>A	XP_011534288.1:p.Val829Glu
XM_011535987.1:c.2105T>A	XP_011534289.1:p.Val702Glu
XM_011535988.1:c.968T>A	XP_011534290.1:p.Val323Glu
NM_001346813.1:c.3827T>A	NP_001333742.1:p.Val1276Glu
NM_001363725.1:c.1577T>A	NP_001350654.1:p.Val526Glu
XM_011535984.2:c.4037T>A	XP_011534286.2:p.Val1346Glu
XM_011535988.3:c.968T>A	XP_011534290.1:p.Val323Glu
XM_017011103.2:c.3938T>A	XP_016866592.1:p.Val1313Glu
XM_017011104.1:c.3908T>A	XP_016866593.1:p.Val1303Glu
XM_017011105.2:c.3878T>A	XP_016866594.1:p.Val1293Glu
XM_017011106.2:c.3749T>A	XP_016866595.1:p.Val1250Glu
XM_017011107.2:c.3728T>A	XP_016866596.1:p.Val1243Glu
XR_002956289.1:n.4120T>A
NM_001363725.2:c.1577T>A	NP_001350654.1:p.Val526Glu
NM_001371656.1:c.3956T>A	NP_001358585.1:p.Val1319Glu
NM_001374820.1:c.3956T>A	NP_001361749.1:p.Val1319Glu
NM_001374828.1:c.4076T>A MANE Select	NP_001361757.1:p.Val1359Glu
NM_017519.3:c.3917T>A	NP_059989.3:p.Val1306Glu