Canonical Allele Identifier: CA366241359

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522114G>C (hg19) ; chr6:g.157200980G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200980G>C , CM000668.2:g.157200980G>C	GRCh38
NC_000006.11:g.157522114G>C , CM000668.1:g.157522114G>C	GRCh37
NC_000006.10:g.157563806G>C	NCBI36
NG_032093.1:g.428051G>C
NG_032093.2:g.428051G>C
NG_066624.1:g.429955G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4596G>C	ENSP00000055163.8:p.Gln1532His
ENST00000414678.8:c.4665G>C	ENSP00000412835.3:p.Gln1555His
ENST00000637015.2:c.4884G>C	ENSP00000489729.2:p.Gln1628His
ENST00000346085.10:c.4635G>C	ENSP00000344546.5:p.Gln1545His
ENST00000350026.10:c.4347G>C	ENSP00000055163.7:p.Gln1449His
ENST00000414678.7:c.2913G>C	ENSP00000412835.2:p.Gln971His
ENST00000635849.1:c.2076G>C	ENSP00000490948.1:p.Gln692His
ENST00000635957.1:c.1707G>C	ENSP00000490385.1:p.Gln569His
ENST00000636227.1:n.3218G>C
ENST00000636254.1:n.675G>C
ENST00000636930.2:c.4755G>C MANE Select	ENSP00000490491.2:p.Gln1585His
ENST00000636940.1:n.2752G>C
ENST00000637015.1:c.2123G>C
ENST00000637568.1:c.2037G>C
ENST00000637741.1:n.1421G>C
ENST00000637810.1:c.2097G>C	ENSP00000489636.1:p.Gln699His
ENST00000637904.1:c.2256G>C	ENSP00000490550.1:p.Gln752His
ENST00000647938.1:c.4386G>C	ENSP00000498155.1:p.Gln1462His
ENST00000346085.9:c.4386G>C	ENSP00000344546.4:p.Gln1462His
ENST00000350026.9:c.4347G>C	ENSP00000055163.7:p.Gln1449His
ENST00000414678.6:c.2913G>C	ENSP00000412835.2:p.Gln971His
NM_017519.2:c.4347G>C	NP_059989.2:p.Gln1449His
NM_020732.3:c.4386G>C	NP_065783.3:p.Gln1462His
XM_005267069.3:c.4506G>C	XP_005267126.2:p.Gln1502His
XM_011535984.1:c.3585G>C	XP_011534286.1:p.Gln1195His
XM_011535985.1:c.3405G>C	XP_011534287.1:p.Gln1135His
XM_011535986.1:c.3165G>C	XP_011534288.1:p.Gln1055His
XM_011535987.1:c.2784G>C	XP_011534289.1:p.Gln928His
XM_011535988.1:c.1647G>C	XP_011534290.1:p.Gln549His
NM_001346813.1:c.4506G>C	NP_001333742.1:p.Gln1502His
NM_001363725.1:c.2256G>C	NP_001350654.1:p.Gln752His
XM_011535984.2:c.4716G>C	XP_011534286.2:p.Gln1572His
XM_011535988.3:c.1647G>C	XP_011534290.1:p.Gln549His
XM_017011103.2:c.4617G>C	XP_016866592.1:p.Gln1539His
XM_017011104.1:c.4587G>C	XP_016866593.1:p.Gln1529His
XM_017011105.2:c.4557G>C	XP_016866594.1:p.Gln1519His
XM_017011106.2:c.4428G>C	XP_016866595.1:p.Gln1476His
XM_017011107.2:c.4407G>C	XP_016866596.1:p.Gln1469His
XR_002956289.1:n.4702G>C
NM_001363725.2:c.2256G>C	NP_001350654.1:p.Gln752His
NM_001371656.1:c.4635G>C	NP_001358585.1:p.Gln1545His
NM_001374820.1:c.4635G>C	NP_001361749.1:p.Gln1545His
NM_001374828.1:c.4755G>C MANE Select	NP_001361757.1:p.Gln1585His
NM_017519.3:c.4596G>C	NP_059989.3:p.Gln1532His