Canonical Allele Identifier: CA366227411

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502167C>G (hg19) ; chr6:g.157181033C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181033C>G , CM000668.2:g.157181033C>G	GRCh38
NC_000006.11:g.157502167C>G , CM000668.1:g.157502167C>G	GRCh37
NC_000006.10:g.157543859C>G	NCBI36
NG_032093.1:g.408104C>G
NG_032093.2:g.408104C>G
NG_066624.1:g.410008C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3410C>G	ENSP00000055163.8:p.Pro1137Arg
ENST00000414678.8:c.3479C>G	ENSP00000412835.3:p.Pro1160Arg
ENST00000637015.2:c.3698C>G	ENSP00000489729.2:p.Pro1233Arg
ENST00000319584.11:c.1583C>G	ENSP00000313006.7:p.Pro528Arg
ENST00000346085.10:c.3449C>G	ENSP00000344546.5:p.Pro1150Arg
ENST00000350026.10:c.3161C>G	ENSP00000055163.7:p.Pro1054Arg
ENST00000414678.7:c.1727C>G	ENSP00000412835.2:p.Pro576Arg
ENST00000635849.1:c.890C>G	ENSP00000490948.1:p.Pro297Arg
ENST00000635957.1:c.524C>G	ENSP00000490385.1:p.Pro175Arg
ENST00000636930.2:c.3569C>G MANE Select	ENSP00000490491.2:p.Pro1190Arg
ENST00000636940.1:n.1566C>G
ENST00000637015.1:c.937C>G
ENST00000637568.1:c.851C>G
ENST00000637741.1:n.235C>G
ENST00000637810.1:c.911C>G	ENSP00000489636.1:p.Pro304Arg
ENST00000637904.1:c.1070C>G	ENSP00000490550.1:p.Pro357Arg
ENST00000647938.1:c.3200C>G	ENSP00000498155.1:p.Pro1067Arg
ENST00000319584.10:c.1586C>G	ENSP00000313006.6:p.Pro529Arg
ENST00000346085.9:c.3200C>G	ENSP00000344546.4:p.Pro1067Arg
ENST00000350026.9:c.3161C>G	ENSP00000055163.7:p.Pro1054Arg
ENST00000400790.3:c.362C>G	ENSP00000383596.3:p.Pro121Arg
ENST00000414678.6:c.1727C>G	ENSP00000412835.2:p.Pro576Arg
ENST00000478761.3:c.771C>G
NM_017519.2:c.3161C>G	NP_059989.2:p.Pro1054Arg
NM_020732.3:c.3200C>G	NP_065783.3:p.Pro1067Arg
XM_005267069.3:c.3320C>G	XP_005267126.2:p.Pro1107Arg
XM_011535984.1:c.2399C>G	XP_011534286.1:p.Pro800Arg
XM_011535985.1:c.2219C>G	XP_011534287.1:p.Pro740Arg
XM_011535986.1:c.1979C>G	XP_011534288.1:p.Pro660Arg
XM_011535987.1:c.1598C>G	XP_011534289.1:p.Pro533Arg
XM_011535988.1:c.461C>G	XP_011534290.1:p.Pro154Arg
NM_001346813.1:c.3320C>G	NP_001333742.1:p.Pro1107Arg
NM_001363725.1:c.1070C>G	NP_001350654.1:p.Pro357Arg
XM_011535984.2:c.3530C>G	XP_011534286.2:p.Pro1177Arg
XM_011535988.3:c.461C>G	XP_011534290.1:p.Pro154Arg
XM_017011103.2:c.3431C>G	XP_016866592.1:p.Pro1144Arg
XM_017011104.1:c.3401C>G	XP_016866593.1:p.Pro1134Arg
XM_017011105.2:c.3371C>G	XP_016866594.1:p.Pro1124Arg
XM_017011106.2:c.3242C>G	XP_016866595.1:p.Pro1081Arg
XM_017011107.2:c.3221C>G	XP_016866596.1:p.Pro1074Arg
XR_002956289.1:n.3613C>G
NM_001363725.2:c.1070C>G	NP_001350654.1:p.Pro357Arg
NM_001371656.1:c.3449C>G	NP_001358585.1:p.Pro1150Arg
NM_001374820.1:c.3449C>G	NP_001361749.1:p.Pro1150Arg
NM_001374828.1:c.3569C>G MANE Select	NP_001361757.1:p.Pro1190Arg
NM_017519.3:c.3410C>G	NP_059989.3:p.Pro1137Arg