Canonical Allele Identifier: CA366241396

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128373864
• gnomAD v4: 6-157200994-C-T
• MyVariant Identifiers: chr6:g.157522128C>T (hg19) ; chr6:g.157200994C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200994C>T , CM000668.2:g.157200994C>T	GRCh38
NC_000006.11:g.157522128C>T , CM000668.1:g.157522128C>T	GRCh37
NC_000006.10:g.157563820C>T	NCBI36
NG_032093.1:g.428065C>T
NG_032093.2:g.428065C>T
NG_066624.1:g.429969C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4610C>T	ENSP00000055163.8:p.Ala1537Val
ENST00000414678.8:c.4679C>T	ENSP00000412835.3:p.Ala1560Val
ENST00000637015.2:c.4898C>T	ENSP00000489729.2:p.Ala1633Val
ENST00000346085.10:c.4649C>T	ENSP00000344546.5:p.Ala1550Val
ENST00000350026.10:c.4361C>T	ENSP00000055163.7:p.Ala1454Val
ENST00000414678.7:c.2927C>T	ENSP00000412835.2:p.Ala976Val
ENST00000635849.1:c.2090C>T	ENSP00000490948.1:p.Ala697Val
ENST00000635957.1:c.1721C>T	ENSP00000490385.1:p.Ala574Val
ENST00000636227.1:n.3232C>T
ENST00000636254.1:n.689C>T
ENST00000636930.2:c.4769C>T MANE Select	ENSP00000490491.2:p.Ala1590Val
ENST00000636940.1:n.2766C>T
ENST00000637015.1:c.2137C>T
ENST00000637568.1:c.2051C>T
ENST00000637741.1:n.1435C>T
ENST00000637810.1:c.2111C>T	ENSP00000489636.1:p.Ala704Val
ENST00000637904.1:c.2270C>T	ENSP00000490550.1:p.Ala757Val
ENST00000647938.1:c.4400C>T	ENSP00000498155.1:p.Ala1467Val
ENST00000346085.9:c.4400C>T	ENSP00000344546.4:p.Ala1467Val
ENST00000350026.9:c.4361C>T	ENSP00000055163.7:p.Ala1454Val
ENST00000414678.6:c.2927C>T	ENSP00000412835.2:p.Ala976Val
NM_017519.2:c.4361C>T	NP_059989.2:p.Ala1454Val
NM_020732.3:c.4400C>T	NP_065783.3:p.Ala1467Val
XM_005267069.3:c.4520C>T	XP_005267126.2:p.Ala1507Val
XM_011535984.1:c.3599C>T	XP_011534286.1:p.Ala1200Val
XM_011535985.1:c.3419C>T	XP_011534287.1:p.Ala1140Val
XM_011535986.1:c.3179C>T	XP_011534288.1:p.Ala1060Val
XM_011535987.1:c.2798C>T	XP_011534289.1:p.Ala933Val
XM_011535988.1:c.1661C>T	XP_011534290.1:p.Ala554Val
NM_001346813.1:c.4520C>T	NP_001333742.1:p.Ala1507Val
NM_001363725.1:c.2270C>T	NP_001350654.1:p.Ala757Val
XM_011535984.2:c.4730C>T	XP_011534286.2:p.Ala1577Val
XM_011535988.3:c.1661C>T	XP_011534290.1:p.Ala554Val
XM_017011103.2:c.4631C>T	XP_016866592.1:p.Ala1544Val
XM_017011104.1:c.4601C>T	XP_016866593.1:p.Ala1534Val
XM_017011105.2:c.4571C>T	XP_016866594.1:p.Ala1524Val
XM_017011106.2:c.4442C>T	XP_016866595.1:p.Ala1481Val
XM_017011107.2:c.4421C>T	XP_016866596.1:p.Ala1474Val
XR_002956289.1:n.4716C>T
NM_001363725.2:c.2270C>T	NP_001350654.1:p.Ala757Val
NM_001371656.1:c.4649C>T	NP_001358585.1:p.Ala1550Val
NM_001374820.1:c.4649C>T	NP_001361749.1:p.Ala1550Val
NM_001374828.1:c.4769C>T MANE Select	NP_001361757.1:p.Ala1590Val
NM_017519.3:c.4610C>T	NP_059989.3:p.Ala1537Val