Canonical Allele Identifier: CA366389293

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554226159
• MyVariant Identifiers: chr6:g.157470078C>T (hg19) ; chr6:g.157148944C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148944C>T , CM000668.2:g.157148944C>T	GRCh38
NC_000006.11:g.157470078C>T , CM000668.1:g.157470078C>T	GRCh37
NC_000006.10:g.157511770C>T	NCBI36
NG_032093.1:g.376015C>T
NG_032093.2:g.376015C>T
NG_066624.1:g.377919C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3082C>T	ENSP00000055163.8:p.Gln1028Ter
ENST00000414678.8:c.2992C>T	ENSP00000412835.3:p.Gln998Ter
ENST00000637015.2:c.3082C>T	ENSP00000489729.2:p.Gln1028Ter
ENST00000319584.11:c.1096C>T	ENSP00000313006.7:p.Gln366Ter
ENST00000346085.10:c.3121C>T	ENSP00000344546.5:p.Gln1041Ter
ENST00000350026.10:c.2833C>T	ENSP00000055163.7:p.Gln945Ter
ENST00000414678.7:c.1240C>T	ENSP00000412835.2:p.Gln414Ter
ENST00000452544.2:n.983C>T
ENST00000635849.1:c.403C>T	ENSP00000490948.1:p.Gln135Ter
ENST00000635957.1:c.37C>T	ENSP00000490385.1:p.Gln13Ter
ENST00000636426.1:n.216C>T
ENST00000636930.2:c.3082C>T MANE Select	ENSP00000490491.2:p.Gln1028Ter
ENST00000637015.1:c.321C>T
ENST00000637568.1:c.125C>T
ENST00000637810.1:c.583C>T	ENSP00000489636.1:p.Gln195Ter
ENST00000637904.1:c.583C>T	ENSP00000490550.1:p.Gln195Ter
ENST00000647938.1:c.2872C>T	ENSP00000498155.1:p.Gln958Ter
ENST00000674190.1:n.1831C>T
ENST00000319584.10:c.1099C>T	ENSP00000313006.6:p.Gln367Ter
ENST00000346085.9:c.2872C>T	ENSP00000344546.4:p.Gln958Ter
ENST00000350026.9:c.2833C>T	ENSP00000055163.7:p.Gln945Ter
ENST00000400790.3:c.34C>T	ENSP00000383596.3:p.Gln12Ter
ENST00000414678.6:c.1240C>T	ENSP00000412835.2:p.Gln414Ter
ENST00000452544.1:n.929C>T
ENST00000478761.3:c.155C>T
NM_017519.2:c.2833C>T	NP_059989.2:p.Gln945Ter
NM_020732.3:c.2872C>T	NP_065783.3:p.Gln958Ter
XM_005267069.3:c.2833C>T	XP_005267126.2:p.Gln945Ter
XM_011535984.1:c.1783C>T	XP_011534286.1:p.Gln595Ter
XM_011535985.1:c.1603C>T	XP_011534287.1:p.Gln535Ter
XM_011535986.1:c.1363C>T	XP_011534288.1:p.Gln455Ter
XM_011535987.1:c.982C>T	XP_011534289.1:p.Gln328Ter
XM_011535988.1:c.-20+15737C>T	XP_011534290.1:n.-20+15737C>T
NM_001346813.1:c.2833C>T	NP_001333742.1:p.Gln945Ter
NM_001363725.1:c.583C>T	NP_001350654.1:p.Gln195Ter
XM_011535984.2:c.2914C>T	XP_011534286.2:p.Gln972Ter
XM_011535988.3:c.-20+15737C>T	XP_011534290.1:n.-20+15737C>T
XM_017011103.2:c.2914C>T	XP_016866592.1:p.Gln972Ter
XM_017011104.1:c.2914C>T	XP_016866593.1:p.Gln972Ter
XM_017011105.2:c.2914C>T	XP_016866594.1:p.Gln972Ter
XM_017011106.2:c.2914C>T	XP_016866595.1:p.Gln972Ter
XM_017011107.2:c.2734C>T	XP_016866596.1:p.Gln912Ter
XR_002956289.1:n.2997C>T
NM_001363725.2:c.583C>T	NP_001350654.1:p.Gln195Ter
NM_001371656.1:c.3121C>T	NP_001358585.1:p.Gln1041Ter
NM_001374820.1:c.3121C>T	NP_001361749.1:p.Gln1041Ter
NM_001374828.1:c.3082C>T MANE Select	NP_001361757.1:p.Gln1028Ter
NM_017519.3:c.3082C>T	NP_059989.3:p.Gln1028Ter