Canonical Allele Identifier: CA366227754

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502205A>G (hg19) ; chr6:g.157181071A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181071A>G , CM000668.2:g.157181071A>G	GRCh38
NC_000006.11:g.157502205A>G , CM000668.1:g.157502205A>G	GRCh37
NC_000006.10:g.157543897A>G	NCBI36
NG_032093.1:g.408142A>G
NG_032093.2:g.408142A>G
NG_066624.1:g.410046A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3448A>G	ENSP00000055163.8:p.Met1150Val
ENST00000414678.8:c.3517A>G	ENSP00000412835.3:p.Met1173Val
ENST00000637015.2:c.3736A>G	ENSP00000489729.2:p.Met1246Val
ENST00000319584.11:c.1621A>G	ENSP00000313006.7:p.Met541Val
ENST00000346085.10:c.3487A>G	ENSP00000344546.5:p.Met1163Val
ENST00000350026.10:c.3199A>G	ENSP00000055163.7:p.Met1067Val
ENST00000414678.7:c.1765A>G	ENSP00000412835.2:p.Met589Val
ENST00000635849.1:c.928A>G	ENSP00000490948.1:p.Met310Val
ENST00000635957.1:c.562A>G	ENSP00000490385.1:p.Met188Val
ENST00000636930.2:c.3607A>G MANE Select	ENSP00000490491.2:p.Met1203Val
ENST00000636940.1:n.1604A>G
ENST00000637015.1:c.975A>G
ENST00000637568.1:c.889A>G
ENST00000637741.1:n.273A>G
ENST00000637810.1:c.949A>G	ENSP00000489636.1:p.Met317Val
ENST00000637904.1:c.1108A>G	ENSP00000490550.1:p.Met370Val
ENST00000647938.1:c.3238A>G	ENSP00000498155.1:p.Met1080Val
ENST00000319584.10:c.1624A>G	ENSP00000313006.6:p.Met542Val
ENST00000346085.9:c.3238A>G	ENSP00000344546.4:p.Met1080Val
ENST00000350026.9:c.3199A>G	ENSP00000055163.7:p.Met1067Val
ENST00000400790.3:c.400A>G	ENSP00000383596.3:p.Met134Val
ENST00000414678.6:c.1765A>G	ENSP00000412835.2:p.Met589Val
ENST00000478761.3:c.809A>G
NM_017519.2:c.3199A>G	NP_059989.2:p.Met1067Val
NM_020732.3:c.3238A>G	NP_065783.3:p.Met1080Val
XM_005267069.3:c.3358A>G	XP_005267126.2:p.Met1120Val
XM_011535984.1:c.2437A>G	XP_011534286.1:p.Met813Val
XM_011535985.1:c.2257A>G	XP_011534287.1:p.Met753Val
XM_011535986.1:c.2017A>G	XP_011534288.1:p.Met673Val
XM_011535987.1:c.1636A>G	XP_011534289.1:p.Met546Val
XM_011535988.1:c.499A>G	XP_011534290.1:p.Met167Val
NM_001346813.1:c.3358A>G	NP_001333742.1:p.Met1120Val
NM_001363725.1:c.1108A>G	NP_001350654.1:p.Met370Val
XM_011535984.2:c.3568A>G	XP_011534286.2:p.Met1190Val
XM_011535988.3:c.499A>G	XP_011534290.1:p.Met167Val
XM_017011103.2:c.3469A>G	XP_016866592.1:p.Met1157Val
XM_017011104.1:c.3439A>G	XP_016866593.1:p.Met1147Val
XM_017011105.2:c.3409A>G	XP_016866594.1:p.Met1137Val
XM_017011106.2:c.3280A>G	XP_016866595.1:p.Met1094Val
XM_017011107.2:c.3259A>G	XP_016866596.1:p.Met1087Val
XR_002956289.1:n.3651A>G
NM_001363725.2:c.1108A>G	NP_001350654.1:p.Met370Val
NM_001371656.1:c.3487A>G	NP_001358585.1:p.Met1163Val
NM_001374820.1:c.3487A>G	NP_001361749.1:p.Met1163Val
NM_001374828.1:c.3607A>G MANE Select	NP_001361757.1:p.Met1203Val
NM_017519.3:c.3448A>G	NP_059989.3:p.Met1150Val