Canonical Allele Identifier: CA366241358

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522113A>C (hg19) ; chr6:g.157200979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200979A>C , CM000668.2:g.157200979A>C	GRCh38
NC_000006.11:g.157522113A>C , CM000668.1:g.157522113A>C	GRCh37
NC_000006.10:g.157563805A>C	NCBI36
NG_032093.1:g.428050A>C
NG_032093.2:g.428050A>C
NG_066624.1:g.429954A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4595A>C	ENSP00000055163.8:p.Gln1532Pro
ENST00000414678.8:c.4664A>C	ENSP00000412835.3:p.Gln1555Pro
ENST00000637015.2:c.4883A>C	ENSP00000489729.2:p.Gln1628Pro
ENST00000346085.10:c.4634A>C	ENSP00000344546.5:p.Gln1545Pro
ENST00000350026.10:c.4346A>C	ENSP00000055163.7:p.Gln1449Pro
ENST00000414678.7:c.2912A>C	ENSP00000412835.2:p.Gln971Pro
ENST00000635849.1:c.2075A>C	ENSP00000490948.1:p.Gln692Pro
ENST00000635957.1:c.1706A>C	ENSP00000490385.1:p.Gln569Pro
ENST00000636227.1:n.3217A>C
ENST00000636254.1:n.674A>C
ENST00000636930.2:c.4754A>C MANE Select	ENSP00000490491.2:p.Gln1585Pro
ENST00000636940.1:n.2751A>C
ENST00000637015.1:c.2122A>C
ENST00000637568.1:c.2036A>C
ENST00000637741.1:n.1420A>C
ENST00000637810.1:c.2096A>C	ENSP00000489636.1:p.Gln699Pro
ENST00000637904.1:c.2255A>C	ENSP00000490550.1:p.Gln752Pro
ENST00000647938.1:c.4385A>C	ENSP00000498155.1:p.Gln1462Pro
ENST00000346085.9:c.4385A>C	ENSP00000344546.4:p.Gln1462Pro
ENST00000350026.9:c.4346A>C	ENSP00000055163.7:p.Gln1449Pro
ENST00000414678.6:c.2912A>C	ENSP00000412835.2:p.Gln971Pro
NM_017519.2:c.4346A>C	NP_059989.2:p.Gln1449Pro
NM_020732.3:c.4385A>C	NP_065783.3:p.Gln1462Pro
XM_005267069.3:c.4505A>C	XP_005267126.2:p.Gln1502Pro
XM_011535984.1:c.3584A>C	XP_011534286.1:p.Gln1195Pro
XM_011535985.1:c.3404A>C	XP_011534287.1:p.Gln1135Pro
XM_011535986.1:c.3164A>C	XP_011534288.1:p.Gln1055Pro
XM_011535987.1:c.2783A>C	XP_011534289.1:p.Gln928Pro
XM_011535988.1:c.1646A>C	XP_011534290.1:p.Gln549Pro
NM_001346813.1:c.4505A>C	NP_001333742.1:p.Gln1502Pro
NM_001363725.1:c.2255A>C	NP_001350654.1:p.Gln752Pro
XM_011535984.2:c.4715A>C	XP_011534286.2:p.Gln1572Pro
XM_011535988.3:c.1646A>C	XP_011534290.1:p.Gln549Pro
XM_017011103.2:c.4616A>C	XP_016866592.1:p.Gln1539Pro
XM_017011104.1:c.4586A>C	XP_016866593.1:p.Gln1529Pro
XM_017011105.2:c.4556A>C	XP_016866594.1:p.Gln1519Pro
XM_017011106.2:c.4427A>C	XP_016866595.1:p.Gln1476Pro
XM_017011107.2:c.4406A>C	XP_016866596.1:p.Gln1469Pro
XR_002956289.1:n.4701A>C
NM_001363725.2:c.2255A>C	NP_001350654.1:p.Gln752Pro
NM_001371656.1:c.4634A>C	NP_001358585.1:p.Gln1545Pro
NM_001374820.1:c.4634A>C	NP_001361749.1:p.Gln1545Pro
NM_001374828.1:c.4754A>C MANE Select	NP_001361757.1:p.Gln1585Pro
NM_017519.3:c.4595A>C	NP_059989.3:p.Gln1532Pro