Canonical Allele Identifier: CA366240909

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157521912A>C (hg19) ; chr6:g.157200778A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200778A>C , CM000668.2:g.157200778A>C	GRCh38
NC_000006.11:g.157521912A>C , CM000668.1:g.157521912A>C	GRCh37
NC_000006.10:g.157563604A>C	NCBI36
NG_032093.1:g.427849A>C
NG_032093.2:g.427849A>C
NG_066624.1:g.429753A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4394A>C	ENSP00000055163.8:p.Gln1465Pro
ENST00000414678.8:c.4463A>C	ENSP00000412835.3:p.Gln1488Pro
ENST00000637015.2:c.4682A>C	ENSP00000489729.2:p.Gln1561Pro
ENST00000346085.10:c.4433A>C	ENSP00000344546.5:p.Gln1478Pro
ENST00000350026.10:c.4145A>C	ENSP00000055163.7:p.Gln1382Pro
ENST00000414678.7:c.2711A>C	ENSP00000412835.2:p.Gln904Pro
ENST00000635849.1:c.1874A>C	ENSP00000490948.1:p.Gln625Pro
ENST00000635957.1:c.1505A>C	ENSP00000490385.1:p.Gln502Pro
ENST00000636227.1:n.3016A>C
ENST00000636254.1:n.473A>C
ENST00000636930.2:c.4553A>C MANE Select	ENSP00000490491.2:p.Gln1518Pro
ENST00000636940.1:n.2550A>C
ENST00000637015.1:c.1921A>C
ENST00000637568.1:c.1835A>C
ENST00000637741.1:n.1219A>C
ENST00000637810.1:c.1895A>C	ENSP00000489636.1:p.Gln632Pro
ENST00000637904.1:c.2054A>C	ENSP00000490550.1:p.Gln685Pro
ENST00000647938.1:c.4184A>C	ENSP00000498155.1:p.Gln1395Pro
ENST00000346085.9:c.4184A>C	ENSP00000344546.4:p.Gln1395Pro
ENST00000350026.9:c.4145A>C	ENSP00000055163.7:p.Gln1382Pro
ENST00000414678.6:c.2711A>C	ENSP00000412835.2:p.Gln904Pro
NM_017519.2:c.4145A>C	NP_059989.2:p.Gln1382Pro
NM_020732.3:c.4184A>C	NP_065783.3:p.Gln1395Pro
XM_005267069.3:c.4304A>C	XP_005267126.2:p.Gln1435Pro
XM_011535984.1:c.3383A>C	XP_011534286.1:p.Gln1128Pro
XM_011535985.1:c.3203A>C	XP_011534287.1:p.Gln1068Pro
XM_011535986.1:c.2963A>C	XP_011534288.1:p.Gln988Pro
XM_011535987.1:c.2582A>C	XP_011534289.1:p.Gln861Pro
XM_011535988.1:c.1445A>C	XP_011534290.1:p.Gln482Pro
NM_001346813.1:c.4304A>C	NP_001333742.1:p.Gln1435Pro
NM_001363725.1:c.2054A>C	NP_001350654.1:p.Gln685Pro
XM_011535984.2:c.4514A>C	XP_011534286.2:p.Gln1505Pro
XM_011535988.3:c.1445A>C	XP_011534290.1:p.Gln482Pro
XM_017011103.2:c.4415A>C	XP_016866592.1:p.Gln1472Pro
XM_017011104.1:c.4385A>C	XP_016866593.1:p.Gln1462Pro
XM_017011105.2:c.4355A>C	XP_016866594.1:p.Gln1452Pro
XM_017011106.2:c.4226A>C	XP_016866595.1:p.Gln1409Pro
XM_017011107.2:c.4205A>C	XP_016866596.1:p.Gln1402Pro
XR_002956289.1:n.4500A>C
NM_001363725.2:c.2054A>C	NP_001350654.1:p.Gln685Pro
NM_001371656.1:c.4433A>C	NP_001358585.1:p.Gln1478Pro
NM_001374820.1:c.4433A>C	NP_001361749.1:p.Gln1478Pro
NM_001374828.1:c.4553A>C MANE Select	NP_001361757.1:p.Gln1518Pro
NM_017519.3:c.4394A>C	NP_059989.3:p.Gln1465Pro