Canonical Allele Identifier: CA4067347

Gene: ARID1B

Linked Data

• dbSNP Id: rs746278639
• ExAC: 6:157502167 C / T
• gnomAD v2: 6-157502167-C-T
• gnomAD v3: 6-157181033-C-T
• gnomAD v4: 6-157181033-C-T
• MyVariant Identifiers: chr6:g.157502167C>T (hg19) ; chr6:g.157181033C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3410C>T	ENSP00000055163.8:p.Pro1137Leu
ENST00000414678.8:c.3479C>T	ENSP00000412835.3:p.Pro1160Leu
ENST00000637015.2:c.3698C>T	ENSP00000489729.2:p.Pro1233Leu
ENST00000319584.11:c.1583C>T	ENSP00000313006.7:p.Pro528Leu
ENST00000346085.10:c.3449C>T	ENSP00000344546.5:p.Pro1150Leu
ENST00000350026.10:c.3161C>T	ENSP00000055163.7:p.Pro1054Leu
ENST00000414678.7:c.1727C>T	ENSP00000412835.2:p.Pro576Leu
ENST00000635849.1:c.890C>T	ENSP00000490948.1:p.Pro297Leu
ENST00000635957.1:c.524C>T	ENSP00000490385.1:p.Pro175Leu
ENST00000636930.2:c.3569C>T MANE Select	ENSP00000490491.2:p.Pro1190Leu
ENST00000636940.1:n.1566C>T
ENST00000637015.1:c.937C>T
ENST00000637568.1:c.851C>T
ENST00000637741.1:n.235C>T
ENST00000637810.1:c.911C>T	ENSP00000489636.1:p.Pro304Leu
ENST00000637904.1:c.1070C>T	ENSP00000490550.1:p.Pro357Leu
ENST00000647938.1:c.3200C>T	ENSP00000498155.1:p.Pro1067Leu
ENST00000319584.10:c.1586C>T	ENSP00000313006.6:p.Pro529Leu
ENST00000346085.9:c.3200C>T	ENSP00000344546.4:p.Pro1067Leu
ENST00000350026.9:c.3161C>T	ENSP00000055163.7:p.Pro1054Leu
ENST00000400790.3:c.362C>T	ENSP00000383596.3:p.Pro121Leu
ENST00000414678.6:c.1727C>T	ENSP00000412835.2:p.Pro576Leu
ENST00000478761.3:c.771C>T
NM_017519.2:c.3161C>T	NP_059989.2:p.Pro1054Leu
NM_020732.3:c.3200C>T	NP_065783.3:p.Pro1067Leu
XM_005267069.3:c.3320C>T	XP_005267126.2:p.Pro1107Leu
XM_011535984.1:c.2399C>T	XP_011534286.1:p.Pro800Leu
XM_011535985.1:c.2219C>T	XP_011534287.1:p.Pro740Leu
XM_011535986.1:c.1979C>T	XP_011534288.1:p.Pro660Leu
XM_011535987.1:c.1598C>T	XP_011534289.1:p.Pro533Leu
XM_011535988.1:c.461C>T	XP_011534290.1:p.Pro154Leu
NM_001346813.1:c.3320C>T	NP_001333742.1:p.Pro1107Leu
NM_001363725.1:c.1070C>T	NP_001350654.1:p.Pro357Leu
XM_011535984.2:c.3530C>T	XP_011534286.2:p.Pro1177Leu
XM_011535988.3:c.461C>T	XP_011534290.1:p.Pro154Leu
XM_017011103.2:c.3431C>T	XP_016866592.1:p.Pro1144Leu
XM_017011104.1:c.3401C>T	XP_016866593.1:p.Pro1134Leu
XM_017011105.2:c.3371C>T	XP_016866594.1:p.Pro1124Leu
XM_017011106.2:c.3242C>T	XP_016866595.1:p.Pro1081Leu
XM_017011107.2:c.3221C>T	XP_016866596.1:p.Pro1074Leu
XR_002956289.1:n.3613C>T
NM_001363725.2:c.1070C>T	NP_001350654.1:p.Pro357Leu
NM_001371656.1:c.3449C>T	NP_001358585.1:p.Pro1150Leu
NM_001374820.1:c.3449C>T	NP_001361749.1:p.Pro1150Leu
NM_001374828.1:c.3569C>T MANE Select	NP_001361757.1:p.Pro1190Leu
NM_017519.3:c.3410C>T	NP_059989.3:p.Pro1137Leu