Canonical Allele Identifier: CA366242684

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376101
• MyVariant Identifiers: chr6:g.157522482C>T (hg19) ; chr6:g.157201348C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201348C>T , CM000668.2:g.157201348C>T	GRCh38
NC_000006.11:g.157522482C>T , CM000668.1:g.157522482C>T	GRCh37
NC_000006.10:g.157564174C>T	NCBI36
NG_032093.1:g.428419C>T
NG_032093.2:g.428419C>T
NG_066624.1:g.430323C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4964C>T	ENSP00000055163.8:p.Pro1655Leu
ENST00000414678.8:c.5033C>T	ENSP00000412835.3:p.Pro1678Leu
ENST00000637015.2:c.5252C>T	ENSP00000489729.2:p.Pro1751Leu
ENST00000346085.10:c.5003C>T	ENSP00000344546.5:p.Pro1668Leu
ENST00000350026.10:c.4715C>T	ENSP00000055163.7:p.Pro1572Leu
ENST00000414678.7:c.3281C>T	ENSP00000412835.2:p.Pro1094Leu
ENST00000635849.1:c.2444C>T	ENSP00000490948.1:p.Pro815Leu
ENST00000635957.1:c.2075C>T	ENSP00000490385.1:p.Pro692Leu
ENST00000636227.1:n.3586C>T
ENST00000636254.1:n.1043C>T
ENST00000636930.2:c.5123C>T MANE Select	ENSP00000490491.2:p.Pro1708Leu
ENST00000636940.1:n.3120C>T
ENST00000637015.1:c.2491C>T
ENST00000637568.1:c.2405C>T
ENST00000637741.1:n.1789C>T
ENST00000637810.1:c.2465C>T	ENSP00000489636.1:p.Pro822Leu
ENST00000637904.1:c.2624C>T	ENSP00000490550.1:p.Pro875Leu
ENST00000647938.1:c.4754C>T	ENSP00000498155.1:p.Pro1585Leu
ENST00000346085.9:c.4754C>T	ENSP00000344546.4:p.Pro1585Leu
ENST00000350026.9:c.4715C>T	ENSP00000055163.7:p.Pro1572Leu
ENST00000414678.6:c.3281C>T	ENSP00000412835.2:p.Pro1094Leu
NM_017519.2:c.4715C>T	NP_059989.2:p.Pro1572Leu
NM_020732.3:c.4754C>T	NP_065783.3:p.Pro1585Leu
XM_005267069.3:c.4874C>T	XP_005267126.2:p.Pro1625Leu
XM_011535984.1:c.3953C>T	XP_011534286.1:p.Pro1318Leu
XM_011535985.1:c.3773C>T	XP_011534287.1:p.Pro1258Leu
XM_011535986.1:c.3533C>T	XP_011534288.1:p.Pro1178Leu
XM_011535987.1:c.3152C>T	XP_011534289.1:p.Pro1051Leu
XM_011535988.1:c.2015C>T	XP_011534290.1:p.Pro672Leu
NM_001346813.1:c.4874C>T	NP_001333742.1:p.Pro1625Leu
NM_001363725.1:c.2624C>T	NP_001350654.1:p.Pro875Leu
XM_011535984.2:c.5084C>T	XP_011534286.2:p.Pro1695Leu
XM_011535988.3:c.2015C>T	XP_011534290.1:p.Pro672Leu
XM_017011103.2:c.4985C>T	XP_016866592.1:p.Pro1662Leu
XM_017011104.1:c.4955C>T	XP_016866593.1:p.Pro1652Leu
XM_017011105.2:c.4925C>T	XP_016866594.1:p.Pro1642Leu
XM_017011106.2:c.4796C>T	XP_016866595.1:p.Pro1599Leu
XM_017011107.2:c.4775C>T	XP_016866596.1:p.Pro1592Leu
XR_002956289.1:n.5070C>T
NM_001363725.2:c.2624C>T	NP_001350654.1:p.Pro875Leu
NM_001371656.1:c.5003C>T	NP_001358585.1:p.Pro1668Leu
NM_001374820.1:c.5003C>T	NP_001361749.1:p.Pro1668Leu
NM_001374828.1:c.5123C>T MANE Select	NP_001361757.1:p.Pro1708Leu
NM_017519.3:c.4964C>T	NP_059989.3:p.Pro1655Leu