Canonical Allele Identifier: CA366234923

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190068-C-G
• MyVariant Identifiers: chr6:g.157511202C>G (hg19) ; chr6:g.157190068C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190068C>G , CM000668.2:g.157190068C>G	GRCh38
NC_000006.11:g.157511202C>G , CM000668.1:g.157511202C>G	GRCh37
NC_000006.10:g.157552894C>G	NCBI36
NG_032093.1:g.417139C>G
NG_032093.2:g.417139C>G
NG_066624.1:g.419043C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3930C>G	ENSP00000055163.8:p.Phe1310Leu
ENST00000414678.8:c.3999C>G	ENSP00000412835.3:p.Phe1333Leu
ENST00000637015.2:c.4218C>G	ENSP00000489729.2:p.Phe1406Leu
ENST00000346085.10:c.3969C>G	ENSP00000344546.5:p.Phe1323Leu
ENST00000350026.10:c.3681C>G	ENSP00000055163.7:p.Phe1227Leu
ENST00000414678.7:c.2247C>G	ENSP00000412835.2:p.Phe749Leu
ENST00000635849.1:c.1410C>G	ENSP00000490948.1:p.Phe470Leu
ENST00000635957.1:c.1041C>G	ENSP00000490385.1:p.Phe347Leu
ENST00000636930.2:c.4089C>G MANE Select	ENSP00000490491.2:p.Phe1363Leu
ENST00000636940.1:n.2086C>G
ENST00000637015.1:c.1457C>G
ENST00000637568.1:c.1371C>G
ENST00000637741.1:n.755C>G
ENST00000637810.1:c.1431C>G	ENSP00000489636.1:p.Phe477Leu
ENST00000637904.1:c.1590C>G	ENSP00000490550.1:p.Phe530Leu
ENST00000647938.1:c.3720C>G	ENSP00000498155.1:p.Phe1240Leu
ENST00000346085.9:c.3720C>G	ENSP00000344546.4:p.Phe1240Leu
ENST00000350026.9:c.3681C>G	ENSP00000055163.7:p.Phe1227Leu
ENST00000414678.6:c.2247C>G	ENSP00000412835.2:p.Phe749Leu
NM_017519.2:c.3681C>G	NP_059989.2:p.Phe1227Leu
NM_020732.3:c.3720C>G	NP_065783.3:p.Phe1240Leu
XM_005267069.3:c.3840C>G	XP_005267126.2:p.Phe1280Leu
XM_011535984.1:c.2919C>G	XP_011534286.1:p.Phe973Leu
XM_011535985.1:c.2739C>G	XP_011534287.1:p.Phe913Leu
XM_011535986.1:c.2499C>G	XP_011534288.1:p.Phe833Leu
XM_011535987.1:c.2118C>G	XP_011534289.1:p.Phe706Leu
XM_011535988.1:c.981C>G	XP_011534290.1:p.Phe327Leu
NM_001346813.1:c.3840C>G	NP_001333742.1:p.Phe1280Leu
NM_001363725.1:c.1590C>G	NP_001350654.1:p.Phe530Leu
XM_011535984.2:c.4050C>G	XP_011534286.2:p.Phe1350Leu
XM_011535988.3:c.981C>G	XP_011534290.1:p.Phe327Leu
XM_017011103.2:c.3951C>G	XP_016866592.1:p.Phe1317Leu
XM_017011104.1:c.3921C>G	XP_016866593.1:p.Phe1307Leu
XM_017011105.2:c.3891C>G	XP_016866594.1:p.Phe1297Leu
XM_017011106.2:c.3762C>G	XP_016866595.1:p.Phe1254Leu
XM_017011107.2:c.3741C>G	XP_016866596.1:p.Phe1247Leu
XR_002956289.1:n.4133C>G
NM_001363725.2:c.1590C>G	NP_001350654.1:p.Phe530Leu
NM_001371656.1:c.3969C>G	NP_001358585.1:p.Phe1323Leu
NM_001374820.1:c.3969C>G	NP_001361749.1:p.Phe1323Leu
NM_001374828.1:c.4089C>G MANE Select	NP_001361757.1:p.Phe1363Leu
NM_017519.3:c.3930C>G	NP_059989.3:p.Phe1310Leu