Canonical Allele Identifier: CA366241925

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522223A>C (hg19) ; chr6:g.157201089A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201089A>C , CM000668.2:g.157201089A>C	GRCh38
NC_000006.11:g.157522223A>C , CM000668.1:g.157522223A>C	GRCh37
NC_000006.10:g.157563915A>C	NCBI36
NG_032093.1:g.428160A>C
NG_032093.2:g.428160A>C
NG_066624.1:g.430064A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4705A>C	ENSP00000055163.8:p.Met1569Leu
ENST00000414678.8:c.4774A>C	ENSP00000412835.3:p.Met1592Leu
ENST00000637015.2:c.4993A>C	ENSP00000489729.2:p.Met1665Leu
ENST00000346085.10:c.4744A>C	ENSP00000344546.5:p.Met1582Leu
ENST00000350026.10:c.4456A>C	ENSP00000055163.7:p.Met1486Leu
ENST00000414678.7:c.3022A>C	ENSP00000412835.2:p.Met1008Leu
ENST00000635849.1:c.2185A>C	ENSP00000490948.1:p.Met729Leu
ENST00000635957.1:c.1816A>C	ENSP00000490385.1:p.Met606Leu
ENST00000636227.1:n.3327A>C
ENST00000636254.1:n.784A>C
ENST00000636930.2:c.4864A>C MANE Select	ENSP00000490491.2:p.Met1622Leu
ENST00000636940.1:n.2861A>C
ENST00000637015.1:c.2232A>C
ENST00000637568.1:c.2146A>C
ENST00000637741.1:n.1530A>C
ENST00000637810.1:c.2206A>C	ENSP00000489636.1:p.Met736Leu
ENST00000637904.1:c.2365A>C	ENSP00000490550.1:p.Met789Leu
ENST00000647938.1:c.4495A>C	ENSP00000498155.1:p.Met1499Leu
ENST00000346085.9:c.4495A>C	ENSP00000344546.4:p.Met1499Leu
ENST00000350026.9:c.4456A>C	ENSP00000055163.7:p.Met1486Leu
ENST00000414678.6:c.3022A>C	ENSP00000412835.2:p.Met1008Leu
NM_017519.2:c.4456A>C	NP_059989.2:p.Met1486Leu
NM_020732.3:c.4495A>C	NP_065783.3:p.Met1499Leu
XM_005267069.3:c.4615A>C	XP_005267126.2:p.Met1539Leu
XM_011535984.1:c.3694A>C	XP_011534286.1:p.Met1232Leu
XM_011535985.1:c.3514A>C	XP_011534287.1:p.Met1172Leu
XM_011535986.1:c.3274A>C	XP_011534288.1:p.Met1092Leu
XM_011535987.1:c.2893A>C	XP_011534289.1:p.Met965Leu
XM_011535988.1:c.1756A>C	XP_011534290.1:p.Met586Leu
NM_001346813.1:c.4615A>C	NP_001333742.1:p.Met1539Leu
NM_001363725.1:c.2365A>C	NP_001350654.1:p.Met789Leu
XM_011535984.2:c.4825A>C	XP_011534286.2:p.Met1609Leu
XM_011535988.3:c.1756A>C	XP_011534290.1:p.Met586Leu
XM_017011103.2:c.4726A>C	XP_016866592.1:p.Met1576Leu
XM_017011104.1:c.4696A>C	XP_016866593.1:p.Met1566Leu
XM_017011105.2:c.4666A>C	XP_016866594.1:p.Met1556Leu
XM_017011106.2:c.4537A>C	XP_016866595.1:p.Met1513Leu
XM_017011107.2:c.4516A>C	XP_016866596.1:p.Met1506Leu
XR_002956289.1:n.4811A>C
NM_001363725.2:c.2365A>C	NP_001350654.1:p.Met789Leu
NM_001371656.1:c.4744A>C	NP_001358585.1:p.Met1582Leu
NM_001374820.1:c.4744A>C	NP_001361749.1:p.Met1582Leu
NM_001374828.1:c.4864A>C MANE Select	NP_001361757.1:p.Met1622Leu
NM_017519.3:c.4705A>C	NP_059989.3:p.Met1569Leu