Canonical Allele Identifier: CA366228453

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502295A>C (hg19) ; chr6:g.157181161A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181161A>C , CM000668.2:g.157181161A>C	GRCh38
NC_000006.11:g.157502295A>C , CM000668.1:g.157502295A>C	GRCh37
NC_000006.10:g.157543987A>C	NCBI36
NG_032093.1:g.408232A>C
NG_032093.2:g.408232A>C
NG_066624.1:g.410136A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3538A>C	ENSP00000055163.8:p.Ile1180Leu
ENST00000414678.8:c.3607A>C	ENSP00000412835.3:p.Ile1203Leu
ENST00000637015.2:c.3826A>C	ENSP00000489729.2:p.Ile1276Leu
ENST00000319584.11:c.1711A>C	ENSP00000313006.7:p.Ile571Leu
ENST00000346085.10:c.3577A>C	ENSP00000344546.5:p.Ile1193Leu
ENST00000350026.10:c.3289A>C	ENSP00000055163.7:p.Ile1097Leu
ENST00000414678.7:c.1855A>C	ENSP00000412835.2:p.Ile619Leu
ENST00000635849.1:c.1018A>C	ENSP00000490948.1:p.Ile340Leu
ENST00000635957.1:c.652A>C	ENSP00000490385.1:p.Ile218Leu
ENST00000636930.2:c.3697A>C MANE Select	ENSP00000490491.2:p.Ile1233Leu
ENST00000636940.1:n.1694A>C
ENST00000637015.1:c.1065A>C
ENST00000637568.1:c.979A>C
ENST00000637741.1:n.363A>C
ENST00000637810.1:c.1039A>C	ENSP00000489636.1:p.Ile347Leu
ENST00000637904.1:c.1198A>C	ENSP00000490550.1:p.Ile400Leu
ENST00000647938.1:c.3328A>C	ENSP00000498155.1:p.Ile1110Leu
ENST00000319584.10:c.1714A>C	ENSP00000313006.6:p.Ile572Leu
ENST00000346085.9:c.3328A>C	ENSP00000344546.4:p.Ile1110Leu
ENST00000350026.9:c.3289A>C	ENSP00000055163.7:p.Ile1097Leu
ENST00000400790.3:c.490A>C	ENSP00000383596.3:p.Ile164Leu
ENST00000414678.6:c.1855A>C	ENSP00000412835.2:p.Ile619Leu
ENST00000478761.3:c.899A>C
NM_017519.2:c.3289A>C	NP_059989.2:p.Ile1097Leu
NM_020732.3:c.3328A>C	NP_065783.3:p.Ile1110Leu
XM_005267069.3:c.3448A>C	XP_005267126.2:p.Ile1150Leu
XM_011535984.1:c.2527A>C	XP_011534286.1:p.Ile843Leu
XM_011535985.1:c.2347A>C	XP_011534287.1:p.Ile783Leu
XM_011535986.1:c.2107A>C	XP_011534288.1:p.Ile703Leu
XM_011535987.1:c.1726A>C	XP_011534289.1:p.Ile576Leu
XM_011535988.1:c.589A>C	XP_011534290.1:p.Ile197Leu
NM_001346813.1:c.3448A>C	NP_001333742.1:p.Ile1150Leu
NM_001363725.1:c.1198A>C	NP_001350654.1:p.Ile400Leu
XM_011535984.2:c.3658A>C	XP_011534286.2:p.Ile1220Leu
XM_011535988.3:c.589A>C	XP_011534290.1:p.Ile197Leu
XM_017011103.2:c.3559A>C	XP_016866592.1:p.Ile1187Leu
XM_017011104.1:c.3529A>C	XP_016866593.1:p.Ile1177Leu
XM_017011105.2:c.3499A>C	XP_016866594.1:p.Ile1167Leu
XM_017011106.2:c.3370A>C	XP_016866595.1:p.Ile1124Leu
XM_017011107.2:c.3349A>C	XP_016866596.1:p.Ile1117Leu
XR_002956289.1:n.3741A>C
NM_001363725.2:c.1198A>C	NP_001350654.1:p.Ile400Leu
NM_001371656.1:c.3577A>C	NP_001358585.1:p.Ile1193Leu
NM_001374820.1:c.3577A>C	NP_001361749.1:p.Ile1193Leu
NM_001374828.1:c.3697A>C MANE Select	NP_001361757.1:p.Ile1233Leu
NM_017519.3:c.3538A>C	NP_059989.3:p.Ile1180Leu