Canonical Allele Identifier: CA366241945

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522226A>C (hg19) ; chr6:g.157201092A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201092A>C , CM000668.2:g.157201092A>C	GRCh38
NC_000006.11:g.157522226A>C , CM000668.1:g.157522226A>C	GRCh37
NC_000006.10:g.157563918A>C	NCBI36
NG_032093.1:g.428163A>C
NG_032093.2:g.428163A>C
NG_066624.1:g.430067A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4708A>C	ENSP00000055163.8:p.Met1570Leu
ENST00000414678.8:c.4777A>C	ENSP00000412835.3:p.Met1593Leu
ENST00000637015.2:c.4996A>C	ENSP00000489729.2:p.Met1666Leu
ENST00000346085.10:c.4747A>C	ENSP00000344546.5:p.Met1583Leu
ENST00000350026.10:c.4459A>C	ENSP00000055163.7:p.Met1487Leu
ENST00000414678.7:c.3025A>C	ENSP00000412835.2:p.Met1009Leu
ENST00000635849.1:c.2188A>C	ENSP00000490948.1:p.Met730Leu
ENST00000635957.1:c.1819A>C	ENSP00000490385.1:p.Met607Leu
ENST00000636227.1:n.3330A>C
ENST00000636254.1:n.787A>C
ENST00000636930.2:c.4867A>C MANE Select	ENSP00000490491.2:p.Met1623Leu
ENST00000636940.1:n.2864A>C
ENST00000637015.1:c.2235A>C
ENST00000637568.1:c.2149A>C
ENST00000637741.1:n.1533A>C
ENST00000637810.1:c.2209A>C	ENSP00000489636.1:p.Met737Leu
ENST00000637904.1:c.2368A>C	ENSP00000490550.1:p.Met790Leu
ENST00000647938.1:c.4498A>C	ENSP00000498155.1:p.Met1500Leu
ENST00000346085.9:c.4498A>C	ENSP00000344546.4:p.Met1500Leu
ENST00000350026.9:c.4459A>C	ENSP00000055163.7:p.Met1487Leu
ENST00000414678.6:c.3025A>C	ENSP00000412835.2:p.Met1009Leu
NM_017519.2:c.4459A>C	NP_059989.2:p.Met1487Leu
NM_020732.3:c.4498A>C	NP_065783.3:p.Met1500Leu
XM_005267069.3:c.4618A>C	XP_005267126.2:p.Met1540Leu
XM_011535984.1:c.3697A>C	XP_011534286.1:p.Met1233Leu
XM_011535985.1:c.3517A>C	XP_011534287.1:p.Met1173Leu
XM_011535986.1:c.3277A>C	XP_011534288.1:p.Met1093Leu
XM_011535987.1:c.2896A>C	XP_011534289.1:p.Met966Leu
XM_011535988.1:c.1759A>C	XP_011534290.1:p.Met587Leu
NM_001346813.1:c.4618A>C	NP_001333742.1:p.Met1540Leu
NM_001363725.1:c.2368A>C	NP_001350654.1:p.Met790Leu
XM_011535984.2:c.4828A>C	XP_011534286.2:p.Met1610Leu
XM_011535988.3:c.1759A>C	XP_011534290.1:p.Met587Leu
XM_017011103.2:c.4729A>C	XP_016866592.1:p.Met1577Leu
XM_017011104.1:c.4699A>C	XP_016866593.1:p.Met1567Leu
XM_017011105.2:c.4669A>C	XP_016866594.1:p.Met1557Leu
XM_017011106.2:c.4540A>C	XP_016866595.1:p.Met1514Leu
XM_017011107.2:c.4519A>C	XP_016866596.1:p.Met1507Leu
XR_002956289.1:n.4814A>C
NM_001363725.2:c.2368A>C	NP_001350654.1:p.Met790Leu
NM_001371656.1:c.4747A>C	NP_001358585.1:p.Met1583Leu
NM_001374820.1:c.4747A>C	NP_001361749.1:p.Met1583Leu
NM_001374828.1:c.4867A>C MANE Select	NP_001361757.1:p.Met1623Leu
NM_017519.3:c.4708A>C	NP_059989.3:p.Met1570Leu