Canonical Allele Identifier: CA366389191

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148896-G-A
• MyVariant Identifiers: chr6:g.157470030G>A (hg19) ; chr6:g.157148896G>A (hg38)
• PubMed: PMID:27479907

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148896G>A , CM000668.2:g.157148896G>A	GRCh38
NC_000006.11:g.157470030G>A , CM000668.1:g.157470030G>A	GRCh37
NC_000006.10:g.157511722G>A	NCBI36
NG_032093.1:g.375967G>A
NG_032093.2:g.375967G>A
NG_066624.1:g.377871G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3034G>A	ENSP00000055163.8:p.Ala1012Thr
ENST00000414678.8:c.2944G>A	ENSP00000412835.3:p.Ala982Thr
ENST00000637015.2:c.3034G>A	ENSP00000489729.2:p.Ala1012Thr
ENST00000319584.11:c.1048G>A	ENSP00000313006.7:p.Ala350Thr
ENST00000346085.10:c.3073G>A	ENSP00000344546.5:p.Ala1025Thr
ENST00000350026.10:c.2785G>A	ENSP00000055163.7:p.Ala929Thr
ENST00000414678.7:c.1192G>A	ENSP00000412835.2:p.Ala398Thr
ENST00000452544.2:n.935G>A
ENST00000635849.1:c.355G>A	ENSP00000490948.1:p.Ala119Thr
ENST00000636426.1:n.168G>A
ENST00000636930.2:c.3034G>A MANE Select	ENSP00000490491.2:p.Ala1012Thr
ENST00000637015.1:c.273G>A
ENST00000637568.1:c.77G>A
ENST00000637810.1:c.535G>A	ENSP00000489636.1:p.Ala179Thr
ENST00000637904.1:c.535G>A	ENSP00000490550.1:p.Ala179Thr
ENST00000647938.1:c.2824G>A	ENSP00000498155.1:p.Ala942Thr
ENST00000674190.1:n.1783G>A
ENST00000319584.10:c.1051G>A	ENSP00000313006.6:p.Ala351Thr
ENST00000346085.9:c.2824G>A	ENSP00000344546.4:p.Ala942Thr
ENST00000350026.9:c.2785G>A	ENSP00000055163.7:p.Ala929Thr
ENST00000414678.6:c.1192G>A	ENSP00000412835.2:p.Ala398Thr
ENST00000452544.1:n.881G>A
ENST00000478761.3:c.107G>A
NM_017519.2:c.2785G>A	NP_059989.2:p.Ala929Thr
NM_020732.3:c.2824G>A	NP_065783.3:p.Ala942Thr
XM_005267069.3:c.2785G>A	XP_005267126.2:p.Ala929Thr
XM_011535984.1:c.1735G>A	XP_011534286.1:p.Ala579Thr
XM_011535985.1:c.1555G>A	XP_011534287.1:p.Ala519Thr
XM_011535986.1:c.1315G>A	XP_011534288.1:p.Ala439Thr
XM_011535987.1:c.934G>A	XP_011534289.1:p.Ala312Thr
XM_011535988.1:c.-20+15689G>A	XP_011534290.1:n.-20+15689G>A
NM_001346813.1:c.2785G>A	NP_001333742.1:p.Ala929Thr
NM_001363725.1:c.535G>A	NP_001350654.1:p.Ala179Thr
XM_011535984.2:c.2866G>A	XP_011534286.2:p.Ala956Thr
XM_011535988.3:c.-20+15689G>A	XP_011534290.1:n.-20+15689G>A
XM_017011103.2:c.2866G>A	XP_016866592.1:p.Ala956Thr
XM_017011104.1:c.2866G>A	XP_016866593.1:p.Ala956Thr
XM_017011105.2:c.2866G>A	XP_016866594.1:p.Ala956Thr
XM_017011106.2:c.2866G>A	XP_016866595.1:p.Ala956Thr
XM_017011107.2:c.2686G>A	XP_016866596.1:p.Ala896Thr
XR_002956289.1:n.2949G>A
NM_001363725.2:c.535G>A	NP_001350654.1:p.Ala179Thr
NM_001371656.1:c.3073G>A	NP_001358585.1:p.Ala1025Thr
NM_001374820.1:c.3073G>A	NP_001361749.1:p.Ala1025Thr
NM_001374828.1:c.3034G>A MANE Select	NP_001361757.1:p.Ala1012Thr
NM_017519.3:c.3034G>A	NP_059989.3:p.Ala1012Thr