Canonical Allele Identifier: CA366234777

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3917T>G	ENSP00000055163.8:p.Val1306Gly
ENST00000414678.8:c.3986T>G	ENSP00000412835.3:p.Val1329Gly
ENST00000637015.2:c.4205T>G	ENSP00000489729.2:p.Val1402Gly
ENST00000346085.10:c.3956T>G	ENSP00000344546.5:p.Val1319Gly
ENST00000350026.10:c.3668T>G	ENSP00000055163.7:p.Val1223Gly
ENST00000414678.7:c.2234T>G	ENSP00000412835.2:p.Val745Gly
ENST00000635849.1:c.1397T>G	ENSP00000490948.1:p.Val466Gly
ENST00000635957.1:c.1028T>G	ENSP00000490385.1:p.Val343Gly
ENST00000636930.2:c.4076T>G MANE Select	ENSP00000490491.2:p.Val1359Gly
ENST00000636940.1:n.2073T>G
ENST00000637015.1:c.1444T>G
ENST00000637568.1:c.1358T>G
ENST00000637741.1:n.742T>G
ENST00000637810.1:c.1418T>G	ENSP00000489636.1:p.Val473Gly
ENST00000637904.1:c.1577T>G	ENSP00000490550.1:p.Val526Gly
ENST00000647938.1:c.3707T>G	ENSP00000498155.1:p.Val1236Gly
ENST00000346085.9:c.3707T>G	ENSP00000344546.4:p.Val1236Gly
ENST00000350026.9:c.3668T>G	ENSP00000055163.7:p.Val1223Gly
ENST00000414678.6:c.2234T>G	ENSP00000412835.2:p.Val745Gly
NM_017519.2:c.3668T>G	NP_059989.2:p.Val1223Gly
NM_020732.3:c.3707T>G	NP_065783.3:p.Val1236Gly
XM_005267069.3:c.3827T>G	XP_005267126.2:p.Val1276Gly
XM_011535984.1:c.2906T>G	XP_011534286.1:p.Val969Gly
XM_011535985.1:c.2726T>G	XP_011534287.1:p.Val909Gly
XM_011535986.1:c.2486T>G	XP_011534288.1:p.Val829Gly
XM_011535987.1:c.2105T>G	XP_011534289.1:p.Val702Gly
XM_011535988.1:c.968T>G	XP_011534290.1:p.Val323Gly
NM_001346813.1:c.3827T>G	NP_001333742.1:p.Val1276Gly
NM_001363725.1:c.1577T>G	NP_001350654.1:p.Val526Gly
XM_011535984.2:c.4037T>G	XP_011534286.2:p.Val1346Gly
XM_011535988.3:c.968T>G	XP_011534290.1:p.Val323Gly
XM_017011103.2:c.3938T>G	XP_016866592.1:p.Val1313Gly
XM_017011104.1:c.3908T>G	XP_016866593.1:p.Val1303Gly
XM_017011105.2:c.3878T>G	XP_016866594.1:p.Val1293Gly
XM_017011106.2:c.3749T>G	XP_016866595.1:p.Val1250Gly
XM_017011107.2:c.3728T>G	XP_016866596.1:p.Val1243Gly
XR_002956289.1:n.4120T>G
NM_001363725.2:c.1577T>G	NP_001350654.1:p.Val526Gly
NM_001371656.1:c.3956T>G	NP_001358585.1:p.Val1319Gly
NM_001374820.1:c.3956T>G	NP_001361749.1:p.Val1319Gly
NM_001374828.1:c.4076T>G MANE Select	NP_001361757.1:p.Val1359Gly
NM_017519.3:c.3917T>G	NP_059989.3:p.Val1306Gly