Canonical Allele Identifier: CA366389020

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469950G>T (hg19) ; chr6:g.157148816G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148816G>T , CM000668.2:g.157148816G>T	GRCh38
NC_000006.11:g.157469950G>T , CM000668.1:g.157469950G>T	GRCh37
NC_000006.10:g.157511642G>T	NCBI36
NG_032093.1:g.375887G>T
NG_032093.2:g.375887G>T
NG_066624.1:g.377791G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2954G>T	ENSP00000055163.8:p.Ser985Ile
ENST00000414678.8:c.2864G>T	ENSP00000412835.3:p.Ser955Ile
ENST00000637015.2:c.2954G>T	ENSP00000489729.2:p.Ser985Ile
ENST00000319584.11:c.968G>T	ENSP00000313006.7:p.Ser323Ile
ENST00000346085.10:c.2993G>T	ENSP00000344546.5:p.Ser998Ile
ENST00000350026.10:c.2705G>T	ENSP00000055163.7:p.Ser902Ile
ENST00000414678.7:c.1112G>T	ENSP00000412835.2:p.Ser371Ile
ENST00000452544.2:n.855G>T
ENST00000635849.1:c.275G>T	ENSP00000490948.1:p.Ser92Ile
ENST00000636426.1:n.88G>T
ENST00000636930.2:c.2954G>T MANE Select	ENSP00000490491.2:p.Ser985Ile
ENST00000637015.1:c.193G>T
ENST00000637810.1:c.455G>T	ENSP00000489636.1:p.Ser152Ile
ENST00000637904.1:c.455G>T	ENSP00000490550.1:p.Ser152Ile
ENST00000647938.1:c.2744G>T	ENSP00000498155.1:p.Ser915Ile
ENST00000674190.1:n.1703G>T
ENST00000319584.10:c.971G>T	ENSP00000313006.6:p.Ser324Ile
ENST00000346085.9:c.2744G>T	ENSP00000344546.4:p.Ser915Ile
ENST00000350026.9:c.2705G>T	ENSP00000055163.7:p.Ser902Ile
ENST00000414678.6:c.1112G>T	ENSP00000412835.2:p.Ser371Ile
ENST00000452544.1:n.801G>T
ENST00000478761.3:c.27G>T
NM_017519.2:c.2705G>T	NP_059989.2:p.Ser902Ile
NM_020732.3:c.2744G>T	NP_065783.3:p.Ser915Ile
XM_005267069.3:c.2705G>T	XP_005267126.2:p.Ser902Ile
XM_011535984.1:c.1655G>T	XP_011534286.1:p.Ser552Ile
XM_011535985.1:c.1475G>T	XP_011534287.1:p.Ser492Ile
XM_011535986.1:c.1235G>T	XP_011534288.1:p.Ser412Ile
XM_011535987.1:c.854G>T	XP_011534289.1:p.Ser285Ile
XM_011535988.1:c.-20+15609G>T	XP_011534290.1:n.-20+15609G>T
NM_001346813.1:c.2705G>T	NP_001333742.1:p.Ser902Ile
NM_001363725.1:c.455G>T	NP_001350654.1:p.Ser152Ile
XM_011535984.2:c.2786G>T	XP_011534286.2:p.Ser929Ile
XM_011535988.3:c.-20+15609G>T	XP_011534290.1:n.-20+15609G>T
XM_017011103.2:c.2786G>T	XP_016866592.1:p.Ser929Ile
XM_017011104.1:c.2786G>T	XP_016866593.1:p.Ser929Ile
XM_017011105.2:c.2786G>T	XP_016866594.1:p.Ser929Ile
XM_017011106.2:c.2786G>T	XP_016866595.1:p.Ser929Ile
XM_017011107.2:c.2606G>T	XP_016866596.1:p.Ser869Ile
XR_002956289.1:n.2869G>T
NM_001363725.2:c.455G>T	NP_001350654.1:p.Ser152Ile
NM_001371656.1:c.2993G>T	NP_001358585.1:p.Ser998Ile
NM_001374820.1:c.2993G>T	NP_001361749.1:p.Ser998Ile
NM_001374828.1:c.2954G>T MANE Select	NP_001361757.1:p.Ser985Ile
NM_017519.3:c.2954G>T	NP_059989.3:p.Ser985Ile