Canonical Allele Identifier: CA366234173

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510860C>T (hg19) ; chr6:g.157189726C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189726C>T , CM000668.2:g.157189726C>T	GRCh38
NC_000006.11:g.157510860C>T , CM000668.1:g.157510860C>T	GRCh37
NC_000006.10:g.157552552C>T	NCBI36
NG_032093.1:g.416797C>T
NG_032093.2:g.416797C>T
NG_066624.1:g.418701C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3845C>T	ENSP00000055163.8:p.Pro1282Leu
ENST00000414678.8:c.3914C>T	ENSP00000412835.3:p.Pro1305Leu
ENST00000637015.2:c.4133C>T	ENSP00000489729.2:p.Pro1378Leu
ENST00000346085.10:c.3884C>T	ENSP00000344546.5:p.Pro1295Leu
ENST00000350026.10:c.3596C>T	ENSP00000055163.7:p.Pro1199Leu
ENST00000414678.7:c.2162C>T	ENSP00000412835.2:p.Pro721Leu
ENST00000635849.1:c.1325C>T	ENSP00000490948.1:p.Pro442Leu
ENST00000635957.1:c.959C>T	ENSP00000490385.1:p.Pro320Leu
ENST00000636930.2:c.4004C>T MANE Select	ENSP00000490491.2:p.Pro1335Leu
ENST00000636940.1:n.2001C>T
ENST00000637015.1:c.1372C>T
ENST00000637568.1:c.1286C>T
ENST00000637741.1:n.670C>T
ENST00000637810.1:c.1346C>T	ENSP00000489636.1:p.Pro449Leu
ENST00000637904.1:c.1505C>T	ENSP00000490550.1:p.Pro502Leu
ENST00000647938.1:c.3635C>T	ENSP00000498155.1:p.Pro1212Leu
ENST00000346085.9:c.3635C>T	ENSP00000344546.4:p.Pro1212Leu
ENST00000350026.9:c.3596C>T	ENSP00000055163.7:p.Pro1199Leu
ENST00000414678.6:c.2162C>T	ENSP00000412835.2:p.Pro721Leu
NM_017519.2:c.3596C>T	NP_059989.2:p.Pro1199Leu
NM_020732.3:c.3635C>T	NP_065783.3:p.Pro1212Leu
XM_005267069.3:c.3755C>T	XP_005267126.2:p.Pro1252Leu
XM_011535984.1:c.2834C>T	XP_011534286.1:p.Pro945Leu
XM_011535985.1:c.2654C>T	XP_011534287.1:p.Pro885Leu
XM_011535986.1:c.2414C>T	XP_011534288.1:p.Pro805Leu
XM_011535987.1:c.2033C>T	XP_011534289.1:p.Pro678Leu
XM_011535988.1:c.896C>T	XP_011534290.1:p.Pro299Leu
NM_001346813.1:c.3755C>T	NP_001333742.1:p.Pro1252Leu
NM_001363725.1:c.1505C>T	NP_001350654.1:p.Pro502Leu
XM_011535984.2:c.3965C>T	XP_011534286.2:p.Pro1322Leu
XM_011535988.3:c.896C>T	XP_011534290.1:p.Pro299Leu
XM_017011103.2:c.3866C>T	XP_016866592.1:p.Pro1289Leu
XM_017011104.1:c.3836C>T	XP_016866593.1:p.Pro1279Leu
XM_017011105.2:c.3806C>T	XP_016866594.1:p.Pro1269Leu
XM_017011106.2:c.3677C>T	XP_016866595.1:p.Pro1226Leu
XM_017011107.2:c.3656C>T	XP_016866596.1:p.Pro1219Leu
XR_002956289.1:n.4048C>T
NM_001363725.2:c.1505C>T	NP_001350654.1:p.Pro502Leu
NM_001371656.1:c.3884C>T	NP_001358585.1:p.Pro1295Leu
NM_001374820.1:c.3884C>T	NP_001361749.1:p.Pro1295Leu
NM_001374828.1:c.4004C>T MANE Select	NP_001361757.1:p.Pro1335Leu
NM_017519.3:c.3845C>T	NP_059989.3:p.Pro1282Leu