Canonical Allele Identifier: CA366241608

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522165G>C (hg19) ; chr6:g.157201031G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201031G>C , CM000668.2:g.157201031G>C	GRCh38
NC_000006.11:g.157522165G>C , CM000668.1:g.157522165G>C	GRCh37
NC_000006.10:g.157563857G>C	NCBI36
NG_032093.1:g.428102G>C
NG_032093.2:g.428102G>C
NG_066624.1:g.430006G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4647G>C	ENSP00000055163.8:p.Gln1549His
ENST00000414678.8:c.4716G>C	ENSP00000412835.3:p.Gln1572His
ENST00000637015.2:c.4935G>C	ENSP00000489729.2:p.Gln1645His
ENST00000346085.10:c.4686G>C	ENSP00000344546.5:p.Gln1562His
ENST00000350026.10:c.4398G>C	ENSP00000055163.7:p.Gln1466His
ENST00000414678.7:c.2964G>C	ENSP00000412835.2:p.Gln988His
ENST00000635849.1:c.2127G>C	ENSP00000490948.1:p.Gln709His
ENST00000635957.1:c.1758G>C	ENSP00000490385.1:p.Gln586His
ENST00000636227.1:n.3269G>C
ENST00000636254.1:n.726G>C
ENST00000636930.2:c.4806G>C MANE Select	ENSP00000490491.2:p.Gln1602His
ENST00000636940.1:n.2803G>C
ENST00000637015.1:c.2174G>C
ENST00000637568.1:c.2088G>C
ENST00000637741.1:n.1472G>C
ENST00000637810.1:c.2148G>C	ENSP00000489636.1:p.Gln716His
ENST00000637904.1:c.2307G>C	ENSP00000490550.1:p.Gln769His
ENST00000647938.1:c.4437G>C	ENSP00000498155.1:p.Gln1479His
ENST00000346085.9:c.4437G>C	ENSP00000344546.4:p.Gln1479His
ENST00000350026.9:c.4398G>C	ENSP00000055163.7:p.Gln1466His
ENST00000414678.6:c.2964G>C	ENSP00000412835.2:p.Gln988His
NM_017519.2:c.4398G>C	NP_059989.2:p.Gln1466His
NM_020732.3:c.4437G>C	NP_065783.3:p.Gln1479His
XM_005267069.3:c.4557G>C	XP_005267126.2:p.Gln1519His
XM_011535984.1:c.3636G>C	XP_011534286.1:p.Gln1212His
XM_011535985.1:c.3456G>C	XP_011534287.1:p.Gln1152His
XM_011535986.1:c.3216G>C	XP_011534288.1:p.Gln1072His
XM_011535987.1:c.2835G>C	XP_011534289.1:p.Gln945His
XM_011535988.1:c.1698G>C	XP_011534290.1:p.Gln566His
NM_001346813.1:c.4557G>C	NP_001333742.1:p.Gln1519His
NM_001363725.1:c.2307G>C	NP_001350654.1:p.Gln769His
XM_011535984.2:c.4767G>C	XP_011534286.2:p.Gln1589His
XM_011535988.3:c.1698G>C	XP_011534290.1:p.Gln566His
XM_017011103.2:c.4668G>C	XP_016866592.1:p.Gln1556His
XM_017011104.1:c.4638G>C	XP_016866593.1:p.Gln1546His
XM_017011105.2:c.4608G>C	XP_016866594.1:p.Gln1536His
XM_017011106.2:c.4479G>C	XP_016866595.1:p.Gln1493His
XM_017011107.2:c.4458G>C	XP_016866596.1:p.Gln1486His
XR_002956289.1:n.4753G>C
NM_001363725.2:c.2307G>C	NP_001350654.1:p.Gln769His
NM_001371656.1:c.4686G>C	NP_001358585.1:p.Gln1562His
NM_001374820.1:c.4686G>C	NP_001361749.1:p.Gln1562His
NM_001374828.1:c.4806G>C MANE Select	NP_001361757.1:p.Gln1602His
NM_017519.3:c.4647G>C	NP_059989.3:p.Gln1549His