Canonical Allele Identifier: CA366241366

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522117T>G (hg19) ; chr6:g.157200983T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200983T>G , CM000668.2:g.157200983T>G	GRCh38
NC_000006.11:g.157522117T>G , CM000668.1:g.157522117T>G	GRCh37
NC_000006.10:g.157563809T>G	NCBI36
NG_032093.1:g.428054T>G
NG_032093.2:g.428054T>G
NG_066624.1:g.429958T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4599T>G	ENSP00000055163.8:p.Asn1533Lys
ENST00000414678.8:c.4668T>G	ENSP00000412835.3:p.Asn1556Lys
ENST00000637015.2:c.4887T>G	ENSP00000489729.2:p.Asn1629Lys
ENST00000346085.10:c.4638T>G	ENSP00000344546.5:p.Asn1546Lys
ENST00000350026.10:c.4350T>G	ENSP00000055163.7:p.Asn1450Lys
ENST00000414678.7:c.2916T>G	ENSP00000412835.2:p.Asn972Lys
ENST00000635849.1:c.2079T>G	ENSP00000490948.1:p.Asn693Lys
ENST00000635957.1:c.1710T>G	ENSP00000490385.1:p.Asn570Lys
ENST00000636227.1:n.3221T>G
ENST00000636254.1:n.678T>G
ENST00000636930.2:c.4758T>G MANE Select	ENSP00000490491.2:p.Asn1586Lys
ENST00000636940.1:n.2755T>G
ENST00000637015.1:c.2126T>G
ENST00000637568.1:c.2040T>G
ENST00000637741.1:n.1424T>G
ENST00000637810.1:c.2100T>G	ENSP00000489636.1:p.Asn700Lys
ENST00000637904.1:c.2259T>G	ENSP00000490550.1:p.Asn753Lys
ENST00000647938.1:c.4389T>G	ENSP00000498155.1:p.Asn1463Lys
ENST00000346085.9:c.4389T>G	ENSP00000344546.4:p.Asn1463Lys
ENST00000350026.9:c.4350T>G	ENSP00000055163.7:p.Asn1450Lys
ENST00000414678.6:c.2916T>G	ENSP00000412835.2:p.Asn972Lys
NM_017519.2:c.4350T>G	NP_059989.2:p.Asn1450Lys
NM_020732.3:c.4389T>G	NP_065783.3:p.Asn1463Lys
XM_005267069.3:c.4509T>G	XP_005267126.2:p.Asn1503Lys
XM_011535984.1:c.3588T>G	XP_011534286.1:p.Asn1196Lys
XM_011535985.1:c.3408T>G	XP_011534287.1:p.Asn1136Lys
XM_011535986.1:c.3168T>G	XP_011534288.1:p.Asn1056Lys
XM_011535987.1:c.2787T>G	XP_011534289.1:p.Asn929Lys
XM_011535988.1:c.1650T>G	XP_011534290.1:p.Asn550Lys
NM_001346813.1:c.4509T>G	NP_001333742.1:p.Asn1503Lys
NM_001363725.1:c.2259T>G	NP_001350654.1:p.Asn753Lys
XM_011535984.2:c.4719T>G	XP_011534286.2:p.Asn1573Lys
XM_011535988.3:c.1650T>G	XP_011534290.1:p.Asn550Lys
XM_017011103.2:c.4620T>G	XP_016866592.1:p.Asn1540Lys
XM_017011104.1:c.4590T>G	XP_016866593.1:p.Asn1530Lys
XM_017011105.2:c.4560T>G	XP_016866594.1:p.Asn1520Lys
XM_017011106.2:c.4431T>G	XP_016866595.1:p.Asn1477Lys
XM_017011107.2:c.4410T>G	XP_016866596.1:p.Asn1470Lys
XR_002956289.1:n.4705T>G
NM_001363725.2:c.2259T>G	NP_001350654.1:p.Asn753Lys
NM_001371656.1:c.4638T>G	NP_001358585.1:p.Asn1546Lys
NM_001374820.1:c.4638T>G	NP_001361749.1:p.Asn1546Lys
NM_001374828.1:c.4758T>G MANE Select	NP_001361757.1:p.Asn1586Lys
NM_017519.3:c.4599T>G	NP_059989.3:p.Asn1533Lys