Canonical Allele Identifier: CA366234170

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128338927
• MyVariant Identifiers: chr6:g.157510859C>T (hg19) ; chr6:g.157189725C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189725C>T , CM000668.2:g.157189725C>T	GRCh38
NC_000006.11:g.157510859C>T , CM000668.1:g.157510859C>T	GRCh37
NC_000006.10:g.157552551C>T	NCBI36
NG_032093.1:g.416796C>T
NG_032093.2:g.416796C>T
NG_066624.1:g.418700C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3844C>T	ENSP00000055163.8:p.Pro1282Ser
ENST00000414678.8:c.3913C>T	ENSP00000412835.3:p.Pro1305Ser
ENST00000637015.2:c.4132C>T	ENSP00000489729.2:p.Pro1378Ser
ENST00000346085.10:c.3883C>T	ENSP00000344546.5:p.Pro1295Ser
ENST00000350026.10:c.3595C>T	ENSP00000055163.7:p.Pro1199Ser
ENST00000414678.7:c.2161C>T	ENSP00000412835.2:p.Pro721Ser
ENST00000635849.1:c.1324C>T	ENSP00000490948.1:p.Pro442Ser
ENST00000635957.1:c.958C>T	ENSP00000490385.1:p.Pro320Ser
ENST00000636930.2:c.4003C>T MANE Select	ENSP00000490491.2:p.Pro1335Ser
ENST00000636940.1:n.2000C>T
ENST00000637015.1:c.1371C>T
ENST00000637568.1:c.1285C>T
ENST00000637741.1:n.669C>T
ENST00000637810.1:c.1345C>T	ENSP00000489636.1:p.Pro449Ser
ENST00000637904.1:c.1504C>T	ENSP00000490550.1:p.Pro502Ser
ENST00000647938.1:c.3634C>T	ENSP00000498155.1:p.Pro1212Ser
ENST00000346085.9:c.3634C>T	ENSP00000344546.4:p.Pro1212Ser
ENST00000350026.9:c.3595C>T	ENSP00000055163.7:p.Pro1199Ser
ENST00000414678.6:c.2161C>T	ENSP00000412835.2:p.Pro721Ser
NM_017519.2:c.3595C>T	NP_059989.2:p.Pro1199Ser
NM_020732.3:c.3634C>T	NP_065783.3:p.Pro1212Ser
XM_005267069.3:c.3754C>T	XP_005267126.2:p.Pro1252Ser
XM_011535984.1:c.2833C>T	XP_011534286.1:p.Pro945Ser
XM_011535985.1:c.2653C>T	XP_011534287.1:p.Pro885Ser
XM_011535986.1:c.2413C>T	XP_011534288.1:p.Pro805Ser
XM_011535987.1:c.2032C>T	XP_011534289.1:p.Pro678Ser
XM_011535988.1:c.895C>T	XP_011534290.1:p.Pro299Ser
NM_001346813.1:c.3754C>T	NP_001333742.1:p.Pro1252Ser
NM_001363725.1:c.1504C>T	NP_001350654.1:p.Pro502Ser
XM_011535984.2:c.3964C>T	XP_011534286.2:p.Pro1322Ser
XM_011535988.3:c.895C>T	XP_011534290.1:p.Pro299Ser
XM_017011103.2:c.3865C>T	XP_016866592.1:p.Pro1289Ser
XM_017011104.1:c.3835C>T	XP_016866593.1:p.Pro1279Ser
XM_017011105.2:c.3805C>T	XP_016866594.1:p.Pro1269Ser
XM_017011106.2:c.3676C>T	XP_016866595.1:p.Pro1226Ser
XM_017011107.2:c.3655C>T	XP_016866596.1:p.Pro1219Ser
XR_002956289.1:n.4047C>T
NM_001363725.2:c.1504C>T	NP_001350654.1:p.Pro502Ser
NM_001371656.1:c.3883C>T	NP_001358585.1:p.Pro1295Ser
NM_001374820.1:c.3883C>T	NP_001361749.1:p.Pro1295Ser
NM_001374828.1:c.4003C>T MANE Select	NP_001361757.1:p.Pro1335Ser
NM_017519.3:c.3844C>T	NP_059989.3:p.Pro1282Ser