Canonical Allele Identifier: CA366234169

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510859C>G (hg19) ; chr6:g.157189725C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3844C>G	ENSP00000055163.8:p.Pro1282Ala
ENST00000414678.8:c.3913C>G	ENSP00000412835.3:p.Pro1305Ala
ENST00000637015.2:c.4132C>G	ENSP00000489729.2:p.Pro1378Ala
ENST00000346085.10:c.3883C>G	ENSP00000344546.5:p.Pro1295Ala
ENST00000350026.10:c.3595C>G	ENSP00000055163.7:p.Pro1199Ala
ENST00000414678.7:c.2161C>G	ENSP00000412835.2:p.Pro721Ala
ENST00000635849.1:c.1324C>G	ENSP00000490948.1:p.Pro442Ala
ENST00000635957.1:c.958C>G	ENSP00000490385.1:p.Pro320Ala
ENST00000636930.2:c.4003C>G MANE Select	ENSP00000490491.2:p.Pro1335Ala
ENST00000636940.1:n.2000C>G
ENST00000637015.1:c.1371C>G
ENST00000637568.1:c.1285C>G
ENST00000637741.1:n.669C>G
ENST00000637810.1:c.1345C>G	ENSP00000489636.1:p.Pro449Ala
ENST00000637904.1:c.1504C>G	ENSP00000490550.1:p.Pro502Ala
ENST00000647938.1:c.3634C>G	ENSP00000498155.1:p.Pro1212Ala
ENST00000346085.9:c.3634C>G	ENSP00000344546.4:p.Pro1212Ala
ENST00000350026.9:c.3595C>G	ENSP00000055163.7:p.Pro1199Ala
ENST00000414678.6:c.2161C>G	ENSP00000412835.2:p.Pro721Ala
NM_017519.2:c.3595C>G	NP_059989.2:p.Pro1199Ala
NM_020732.3:c.3634C>G	NP_065783.3:p.Pro1212Ala
XM_005267069.3:c.3754C>G	XP_005267126.2:p.Pro1252Ala
XM_011535984.1:c.2833C>G	XP_011534286.1:p.Pro945Ala
XM_011535985.1:c.2653C>G	XP_011534287.1:p.Pro885Ala
XM_011535986.1:c.2413C>G	XP_011534288.1:p.Pro805Ala
XM_011535987.1:c.2032C>G	XP_011534289.1:p.Pro678Ala
XM_011535988.1:c.895C>G	XP_011534290.1:p.Pro299Ala
NM_001346813.1:c.3754C>G	NP_001333742.1:p.Pro1252Ala
NM_001363725.1:c.1504C>G	NP_001350654.1:p.Pro502Ala
XM_011535984.2:c.3964C>G	XP_011534286.2:p.Pro1322Ala
XM_011535988.3:c.895C>G	XP_011534290.1:p.Pro299Ala
XM_017011103.2:c.3865C>G	XP_016866592.1:p.Pro1289Ala
XM_017011104.1:c.3835C>G	XP_016866593.1:p.Pro1279Ala
XM_017011105.2:c.3805C>G	XP_016866594.1:p.Pro1269Ala
XM_017011106.2:c.3676C>G	XP_016866595.1:p.Pro1226Ala
XM_017011107.2:c.3655C>G	XP_016866596.1:p.Pro1219Ala
XR_002956289.1:n.4047C>G
NM_001363725.2:c.1504C>G	NP_001350654.1:p.Pro502Ala
NM_001371656.1:c.3883C>G	NP_001358585.1:p.Pro1295Ala
NM_001374820.1:c.3883C>G	NP_001361749.1:p.Pro1295Ala
NM_001374828.1:c.4003C>G MANE Select	NP_001361757.1:p.Pro1335Ala
NM_017519.3:c.3844C>G	NP_059989.3:p.Pro1282Ala