Canonical Allele Identifier: CA366227766

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502206T>G (hg19) ; chr6:g.157181072T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181072T>G , CM000668.2:g.157181072T>G	GRCh38
NC_000006.11:g.157502206T>G , CM000668.1:g.157502206T>G	GRCh37
NC_000006.10:g.157543898T>G	NCBI36
NG_032093.1:g.408143T>G
NG_032093.2:g.408143T>G
NG_066624.1:g.410047T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3449T>G	ENSP00000055163.8:p.Met1150Arg
ENST00000414678.8:c.3518T>G	ENSP00000412835.3:p.Met1173Arg
ENST00000637015.2:c.3737T>G	ENSP00000489729.2:p.Met1246Arg
ENST00000319584.11:c.1622T>G	ENSP00000313006.7:p.Met541Arg
ENST00000346085.10:c.3488T>G	ENSP00000344546.5:p.Met1163Arg
ENST00000350026.10:c.3200T>G	ENSP00000055163.7:p.Met1067Arg
ENST00000414678.7:c.1766T>G	ENSP00000412835.2:p.Met589Arg
ENST00000635849.1:c.929T>G	ENSP00000490948.1:p.Met310Arg
ENST00000635957.1:c.563T>G	ENSP00000490385.1:p.Met188Arg
ENST00000636930.2:c.3608T>G MANE Select	ENSP00000490491.2:p.Met1203Arg
ENST00000636940.1:n.1605T>G
ENST00000637015.1:c.976T>G
ENST00000637568.1:c.890T>G
ENST00000637741.1:n.274T>G
ENST00000637810.1:c.950T>G	ENSP00000489636.1:p.Met317Arg
ENST00000637904.1:c.1109T>G	ENSP00000490550.1:p.Met370Arg
ENST00000647938.1:c.3239T>G	ENSP00000498155.1:p.Met1080Arg
ENST00000319584.10:c.1625T>G	ENSP00000313006.6:p.Met542Arg
ENST00000346085.9:c.3239T>G	ENSP00000344546.4:p.Met1080Arg
ENST00000350026.9:c.3200T>G	ENSP00000055163.7:p.Met1067Arg
ENST00000400790.3:c.401T>G	ENSP00000383596.3:p.Met134Arg
ENST00000414678.6:c.1766T>G	ENSP00000412835.2:p.Met589Arg
ENST00000478761.3:c.810T>G
NM_017519.2:c.3200T>G	NP_059989.2:p.Met1067Arg
NM_020732.3:c.3239T>G	NP_065783.3:p.Met1080Arg
XM_005267069.3:c.3359T>G	XP_005267126.2:p.Met1120Arg
XM_011535984.1:c.2438T>G	XP_011534286.1:p.Met813Arg
XM_011535985.1:c.2258T>G	XP_011534287.1:p.Met753Arg
XM_011535986.1:c.2018T>G	XP_011534288.1:p.Met673Arg
XM_011535987.1:c.1637T>G	XP_011534289.1:p.Met546Arg
XM_011535988.1:c.500T>G	XP_011534290.1:p.Met167Arg
NM_001346813.1:c.3359T>G	NP_001333742.1:p.Met1120Arg
NM_001363725.1:c.1109T>G	NP_001350654.1:p.Met370Arg
XM_011535984.2:c.3569T>G	XP_011534286.2:p.Met1190Arg
XM_011535988.3:c.500T>G	XP_011534290.1:p.Met167Arg
XM_017011103.2:c.3470T>G	XP_016866592.1:p.Met1157Arg
XM_017011104.1:c.3440T>G	XP_016866593.1:p.Met1147Arg
XM_017011105.2:c.3410T>G	XP_016866594.1:p.Met1137Arg
XM_017011106.2:c.3281T>G	XP_016866595.1:p.Met1094Arg
XM_017011107.2:c.3260T>G	XP_016866596.1:p.Met1087Arg
XR_002956289.1:n.3652T>G
NM_001363725.2:c.1109T>G	NP_001350654.1:p.Met370Arg
NM_001371656.1:c.3488T>G	NP_001358585.1:p.Met1163Arg
NM_001374820.1:c.3488T>G	NP_001361749.1:p.Met1163Arg
NM_001374828.1:c.3608T>G MANE Select	NP_001361757.1:p.Met1203Arg
NM_017519.3:c.3449T>G	NP_059989.3:p.Met1150Arg