Canonical Allele Identifier: CA366241905

Gene: ARID1B

Linked Data

• dbSNP Id: rs1320072402
• MyVariant Identifiers: chr6:g.157522220G>C (hg19) ; chr6:g.157201086G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201086G>C , CM000668.2:g.157201086G>C	GRCh38
NC_000006.11:g.157522220G>C , CM000668.1:g.157522220G>C	GRCh37
NC_000006.10:g.157563912G>C	NCBI36
NG_032093.1:g.428157G>C
NG_032093.2:g.428157G>C
NG_066624.1:g.430061G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4702G>C	ENSP00000055163.8:p.Asp1568His
ENST00000414678.8:c.4771G>C	ENSP00000412835.3:p.Asp1591His
ENST00000637015.2:c.4990G>C	ENSP00000489729.2:p.Asp1664His
ENST00000346085.10:c.4741G>C	ENSP00000344546.5:p.Asp1581His
ENST00000350026.10:c.4453G>C	ENSP00000055163.7:p.Asp1485His
ENST00000414678.7:c.3019G>C	ENSP00000412835.2:p.Asp1007His
ENST00000635849.1:c.2182G>C	ENSP00000490948.1:p.Asp728His
ENST00000635957.1:c.1813G>C	ENSP00000490385.1:p.Asp605His
ENST00000636227.1:n.3324G>C
ENST00000636254.1:n.781G>C
ENST00000636930.2:c.4861G>C MANE Select	ENSP00000490491.2:p.Asp1621His
ENST00000636940.1:n.2858G>C
ENST00000637015.1:c.2229G>C
ENST00000637568.1:c.2143G>C
ENST00000637741.1:n.1527G>C
ENST00000637810.1:c.2203G>C	ENSP00000489636.1:p.Asp735His
ENST00000637904.1:c.2362G>C	ENSP00000490550.1:p.Asp788His
ENST00000647938.1:c.4492G>C	ENSP00000498155.1:p.Asp1498His
ENST00000346085.9:c.4492G>C	ENSP00000344546.4:p.Asp1498His
ENST00000350026.9:c.4453G>C	ENSP00000055163.7:p.Asp1485His
ENST00000414678.6:c.3019G>C	ENSP00000412835.2:p.Asp1007His
NM_017519.2:c.4453G>C	NP_059989.2:p.Asp1485His
NM_020732.3:c.4492G>C	NP_065783.3:p.Asp1498His
XM_005267069.3:c.4612G>C	XP_005267126.2:p.Asp1538His
XM_011535984.1:c.3691G>C	XP_011534286.1:p.Asp1231His
XM_011535985.1:c.3511G>C	XP_011534287.1:p.Asp1171His
XM_011535986.1:c.3271G>C	XP_011534288.1:p.Asp1091His
XM_011535987.1:c.2890G>C	XP_011534289.1:p.Asp964His
XM_011535988.1:c.1753G>C	XP_011534290.1:p.Asp585His
NM_001346813.1:c.4612G>C	NP_001333742.1:p.Asp1538His
NM_001363725.1:c.2362G>C	NP_001350654.1:p.Asp788His
XM_011535984.2:c.4822G>C	XP_011534286.2:p.Asp1608His
XM_011535988.3:c.1753G>C	XP_011534290.1:p.Asp585His
XM_017011103.2:c.4723G>C	XP_016866592.1:p.Asp1575His
XM_017011104.1:c.4693G>C	XP_016866593.1:p.Asp1565His
XM_017011105.2:c.4663G>C	XP_016866594.1:p.Asp1555His
XM_017011106.2:c.4534G>C	XP_016866595.1:p.Asp1512His
XM_017011107.2:c.4513G>C	XP_016866596.1:p.Asp1505His
XR_002956289.1:n.4808G>C
NM_001363725.2:c.2362G>C	NP_001350654.1:p.Asp788His
NM_001371656.1:c.4741G>C	NP_001358585.1:p.Asp1581His
NM_001374820.1:c.4741G>C	NP_001361749.1:p.Asp1581His
NM_001374828.1:c.4861G>C MANE Select	NP_001361757.1:p.Asp1621His
NM_017519.3:c.4702G>C	NP_059989.3:p.Asp1568His