Canonical Allele Identifier: CA366227734

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317195
• MyVariant Identifiers: chr6:g.157502204C>G (hg19) ; chr6:g.157181070C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181070C>G , CM000668.2:g.157181070C>G	GRCh38
NC_000006.11:g.157502204C>G , CM000668.1:g.157502204C>G	GRCh37
NC_000006.10:g.157543896C>G	NCBI36
NG_032093.1:g.408141C>G
NG_032093.2:g.408141C>G
NG_066624.1:g.410045C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3447C>G	ENSP00000055163.8:p.Phe1149Leu
ENST00000414678.8:c.3516C>G	ENSP00000412835.3:p.Phe1172Leu
ENST00000637015.2:c.3735C>G	ENSP00000489729.2:p.Phe1245Leu
ENST00000319584.11:c.1620C>G	ENSP00000313006.7:p.Phe540Leu
ENST00000346085.10:c.3486C>G	ENSP00000344546.5:p.Phe1162Leu
ENST00000350026.10:c.3198C>G	ENSP00000055163.7:p.Phe1066Leu
ENST00000414678.7:c.1764C>G	ENSP00000412835.2:p.Phe588Leu
ENST00000635849.1:c.927C>G	ENSP00000490948.1:p.Phe309Leu
ENST00000635957.1:c.561C>G	ENSP00000490385.1:p.Phe187Leu
ENST00000636930.2:c.3606C>G MANE Select	ENSP00000490491.2:p.Phe1202Leu
ENST00000636940.1:n.1603C>G
ENST00000637015.1:c.974C>G
ENST00000637568.1:c.888C>G
ENST00000637741.1:n.272C>G
ENST00000637810.1:c.948C>G	ENSP00000489636.1:p.Phe316Leu
ENST00000637904.1:c.1107C>G	ENSP00000490550.1:p.Phe369Leu
ENST00000647938.1:c.3237C>G	ENSP00000498155.1:p.Phe1079Leu
ENST00000319584.10:c.1623C>G	ENSP00000313006.6:p.Phe541Leu
ENST00000346085.9:c.3237C>G	ENSP00000344546.4:p.Phe1079Leu
ENST00000350026.9:c.3198C>G	ENSP00000055163.7:p.Phe1066Leu
ENST00000400790.3:c.399C>G	ENSP00000383596.3:p.Phe133Leu
ENST00000414678.6:c.1764C>G	ENSP00000412835.2:p.Phe588Leu
ENST00000478761.3:c.808C>G
NM_017519.2:c.3198C>G	NP_059989.2:p.Phe1066Leu
NM_020732.3:c.3237C>G	NP_065783.3:p.Phe1079Leu
XM_005267069.3:c.3357C>G	XP_005267126.2:p.Phe1119Leu
XM_011535984.1:c.2436C>G	XP_011534286.1:p.Phe812Leu
XM_011535985.1:c.2256C>G	XP_011534287.1:p.Phe752Leu
XM_011535986.1:c.2016C>G	XP_011534288.1:p.Phe672Leu
XM_011535987.1:c.1635C>G	XP_011534289.1:p.Phe545Leu
XM_011535988.1:c.498C>G	XP_011534290.1:p.Phe166Leu
NM_001346813.1:c.3357C>G	NP_001333742.1:p.Phe1119Leu
NM_001363725.1:c.1107C>G	NP_001350654.1:p.Phe369Leu
XM_011535984.2:c.3567C>G	XP_011534286.2:p.Phe1189Leu
XM_011535988.3:c.498C>G	XP_011534290.1:p.Phe166Leu
XM_017011103.2:c.3468C>G	XP_016866592.1:p.Phe1156Leu
XM_017011104.1:c.3438C>G	XP_016866593.1:p.Phe1146Leu
XM_017011105.2:c.3408C>G	XP_016866594.1:p.Phe1136Leu
XM_017011106.2:c.3279C>G	XP_016866595.1:p.Phe1093Leu
XM_017011107.2:c.3258C>G	XP_016866596.1:p.Phe1086Leu
XR_002956289.1:n.3650C>G
NM_001363725.2:c.1107C>G	NP_001350654.1:p.Phe369Leu
NM_001371656.1:c.3486C>G	NP_001358585.1:p.Phe1162Leu
NM_001374820.1:c.3486C>G	NP_001361749.1:p.Phe1162Leu
NM_001374828.1:c.3606C>G MANE Select	NP_001361757.1:p.Phe1202Leu
NM_017519.3:c.3447C>G	NP_059989.3:p.Phe1149Leu