Canonical Allele Identifier: CA366227758

Gene: ARID1B

Linked Data

• dbSNP Id: rs760633180
• gnomAD v2: 6-157502205-A-T
• gnomAD v4: 6-157181071-A-T
• MyVariant Identifiers: chr6:g.157502205A>T (hg19) ; chr6:g.157181071A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3448A>T	ENSP00000055163.8:p.Met1150Leu
ENST00000414678.8:c.3517A>T	ENSP00000412835.3:p.Met1173Leu
ENST00000637015.2:c.3736A>T	ENSP00000489729.2:p.Met1246Leu
ENST00000319584.11:c.1621A>T	ENSP00000313006.7:p.Met541Leu
ENST00000346085.10:c.3487A>T	ENSP00000344546.5:p.Met1163Leu
ENST00000350026.10:c.3199A>T	ENSP00000055163.7:p.Met1067Leu
ENST00000414678.7:c.1765A>T	ENSP00000412835.2:p.Met589Leu
ENST00000635849.1:c.928A>T	ENSP00000490948.1:p.Met310Leu
ENST00000635957.1:c.562A>T	ENSP00000490385.1:p.Met188Leu
ENST00000636930.2:c.3607A>T MANE Select	ENSP00000490491.2:p.Met1203Leu
ENST00000636940.1:n.1604A>T
ENST00000637015.1:c.975A>T
ENST00000637568.1:c.889A>T
ENST00000637741.1:n.273A>T
ENST00000637810.1:c.949A>T	ENSP00000489636.1:p.Met317Leu
ENST00000637904.1:c.1108A>T	ENSP00000490550.1:p.Met370Leu
ENST00000647938.1:c.3238A>T	ENSP00000498155.1:p.Met1080Leu
ENST00000319584.10:c.1624A>T	ENSP00000313006.6:p.Met542Leu
ENST00000346085.9:c.3238A>T	ENSP00000344546.4:p.Met1080Leu
ENST00000350026.9:c.3199A>T	ENSP00000055163.7:p.Met1067Leu
ENST00000400790.3:c.400A>T	ENSP00000383596.3:p.Met134Leu
ENST00000414678.6:c.1765A>T	ENSP00000412835.2:p.Met589Leu
ENST00000478761.3:c.809A>T
NM_017519.2:c.3199A>T	NP_059989.2:p.Met1067Leu
NM_020732.3:c.3238A>T	NP_065783.3:p.Met1080Leu
XM_005267069.3:c.3358A>T	XP_005267126.2:p.Met1120Leu
XM_011535984.1:c.2437A>T	XP_011534286.1:p.Met813Leu
XM_011535985.1:c.2257A>T	XP_011534287.1:p.Met753Leu
XM_011535986.1:c.2017A>T	XP_011534288.1:p.Met673Leu
XM_011535987.1:c.1636A>T	XP_011534289.1:p.Met546Leu
XM_011535988.1:c.499A>T	XP_011534290.1:p.Met167Leu
NM_001346813.1:c.3358A>T	NP_001333742.1:p.Met1120Leu
NM_001363725.1:c.1108A>T	NP_001350654.1:p.Met370Leu
XM_011535984.2:c.3568A>T	XP_011534286.2:p.Met1190Leu
XM_011535988.3:c.499A>T	XP_011534290.1:p.Met167Leu
XM_017011103.2:c.3469A>T	XP_016866592.1:p.Met1157Leu
XM_017011104.1:c.3439A>T	XP_016866593.1:p.Met1147Leu
XM_017011105.2:c.3409A>T	XP_016866594.1:p.Met1137Leu
XM_017011106.2:c.3280A>T	XP_016866595.1:p.Met1094Leu
XM_017011107.2:c.3259A>T	XP_016866596.1:p.Met1087Leu
XR_002956289.1:n.3651A>T
NM_001363725.2:c.1108A>T	NP_001350654.1:p.Met370Leu
NM_001371656.1:c.3487A>T	NP_001358585.1:p.Met1163Leu
NM_001374820.1:c.3487A>T	NP_001361749.1:p.Met1163Leu
NM_001374828.1:c.3607A>T MANE Select	NP_001361757.1:p.Met1203Leu
NM_017519.3:c.3448A>T	NP_059989.3:p.Met1150Leu