Canonical Allele Identifier: CA452780823

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502282C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181148C>A , CM000668.2:g.157181148C>A	GRCh38
NC_000006.11:g.157502282C>A , CM000668.1:g.157502282C>A	GRCh37
NC_000006.10:g.157543974C>A	NCBI36
NG_032093.1:g.408219C>A
NG_032093.2:g.408219C>A
NG_066624.1:g.410123C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3525C>A	ENSP00000055163.8:p.Val1175=
ENST00000414678.8:c.3594C>A	ENSP00000412835.3:p.Val1198=
ENST00000637015.2:c.3813C>A	ENSP00000489729.2:p.Val1271=
ENST00000319584.11:c.1698C>A	ENSP00000313006.7:p.Val566=
ENST00000346085.10:c.3564C>A	ENSP00000344546.5:p.Val1188=
ENST00000350026.10:c.3276C>A	ENSP00000055163.7:p.Val1092=
ENST00000414678.7:c.1842C>A	ENSP00000412835.2:p.Val614=
ENST00000635849.1:c.1005C>A	ENSP00000490948.1:p.Val335=
ENST00000635957.1:c.639C>A	ENSP00000490385.1:p.Val213=
ENST00000636930.2:c.3684C>A MANE Select	ENSP00000490491.2:p.Val1228=
ENST00000636940.1:n.1681C>A
ENST00000637015.1:c.1052C>A
ENST00000637568.1:c.966C>A
ENST00000637741.1:n.350C>A
ENST00000637810.1:c.1026C>A	ENSP00000489636.1:p.Val342=
ENST00000637904.1:c.1185C>A	ENSP00000490550.1:p.Val395=
ENST00000647938.1:c.3315C>A	ENSP00000498155.1:p.Val1105=
ENST00000319584.10:c.1701C>A	ENSP00000313006.6:p.Val567=
ENST00000346085.9:c.3315C>A	ENSP00000344546.4:p.Val1105=
ENST00000350026.9:c.3276C>A	ENSP00000055163.7:p.Val1092=
ENST00000400790.3:c.477C>A	ENSP00000383596.3:p.Val159=
ENST00000414678.6:c.1842C>A	ENSP00000412835.2:p.Val614=
ENST00000478761.3:c.886C>A
NM_017519.2:c.3276C>A	NP_059989.2:p.Val1092=
NM_020732.3:c.3315C>A	NP_065783.3:p.Val1105=
XM_005267069.3:c.3435C>A	XP_005267126.2:p.Val1145=
XM_011535984.1:c.2514C>A	XP_011534286.1:p.Val838=
XM_011535985.1:c.2334C>A	XP_011534287.1:p.Val778=
XM_011535986.1:c.2094C>A	XP_011534288.1:p.Val698=
XM_011535987.1:c.1713C>A	XP_011534289.1:p.Val571=
XM_011535988.1:c.576C>A	XP_011534290.1:p.Val192=
NM_001346813.1:c.3435C>A	NP_001333742.1:p.Val1145=
NM_001363725.1:c.1185C>A	NP_001350654.1:p.Val395=
XM_011535984.2:c.3645C>A	XP_011534286.2:p.Val1215=
XM_011535988.3:c.576C>A	XP_011534290.1:p.Val192=
XM_017011103.2:c.3546C>A	XP_016866592.1:p.Val1182=
XM_017011104.1:c.3516C>A	XP_016866593.1:p.Val1172=
XM_017011105.2:c.3486C>A	XP_016866594.1:p.Val1162=
XM_017011106.2:c.3357C>A	XP_016866595.1:p.Val1119=
XM_017011107.2:c.3336C>A	XP_016866596.1:p.Val1112=
XR_002956289.1:n.3728C>A
NM_001363725.2:c.1185C>A	NP_001350654.1:p.Val395=
NM_001371656.1:c.3564C>A	NP_001358585.1:p.Val1188=
NM_001374820.1:c.3564C>A	NP_001361749.1:p.Val1188=
NM_001374828.1:c.3684C>A MANE Select	NP_001361757.1:p.Val1228=
NM_017519.3:c.3525C>A	NP_059989.3:p.Val1175=