Canonical Allele Identifier: CA452990149

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470077A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148943A>C , CM000668.2:g.157148943A>C	GRCh38
NC_000006.11:g.157470077A>C , CM000668.1:g.157470077A>C	GRCh37
NC_000006.10:g.157511769A>C	NCBI36
NG_032093.1:g.376014A>C
NG_032093.2:g.376014A>C
NG_066624.1:g.377918A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3081A>C	ENSP00000055163.8:p.Ala1027=
ENST00000414678.8:c.2991A>C	ENSP00000412835.3:p.Ala997=
ENST00000637015.2:c.3081A>C	ENSP00000489729.2:p.Ala1027=
ENST00000319584.11:c.1095A>C	ENSP00000313006.7:p.Ala365=
ENST00000346085.10:c.3120A>C	ENSP00000344546.5:p.Ala1040=
ENST00000350026.10:c.2832A>C	ENSP00000055163.7:p.Ala944=
ENST00000414678.7:c.1239A>C	ENSP00000412835.2:p.Ala413=
ENST00000452544.2:n.982A>C
ENST00000635849.1:c.402A>C	ENSP00000490948.1:p.Ala134=
ENST00000635957.1:c.36A>C	ENSP00000490385.1:p.Ala12=
ENST00000636426.1:n.215A>C
ENST00000636930.2:c.3081A>C MANE Select	ENSP00000490491.2:p.Ala1027=
ENST00000637015.1:c.320A>C
ENST00000637568.1:c.124A>C
ENST00000637810.1:c.582A>C	ENSP00000489636.1:p.Ala194=
ENST00000637904.1:c.582A>C	ENSP00000490550.1:p.Ala194=
ENST00000647938.1:c.2871A>C	ENSP00000498155.1:p.Ala957=
ENST00000674190.1:n.1830A>C
ENST00000319584.10:c.1098A>C	ENSP00000313006.6:p.Ala366=
ENST00000346085.9:c.2871A>C	ENSP00000344546.4:p.Ala957=
ENST00000350026.9:c.2832A>C	ENSP00000055163.7:p.Ala944=
ENST00000400790.3:c.33A>C	ENSP00000383596.3:p.Ala11=
ENST00000414678.6:c.1239A>C	ENSP00000412835.2:p.Ala413=
ENST00000452544.1:n.928A>C
ENST00000478761.3:c.154A>C
NM_017519.2:c.2832A>C	NP_059989.2:p.Ala944=
NM_020732.3:c.2871A>C	NP_065783.3:p.Ala957=
XM_005267069.3:c.2832A>C	XP_005267126.2:p.Ala944=
XM_011535984.1:c.1782A>C	XP_011534286.1:p.Ala594=
XM_011535985.1:c.1602A>C	XP_011534287.1:p.Ala534=
XM_011535986.1:c.1362A>C	XP_011534288.1:p.Ala454=
XM_011535987.1:c.981A>C	XP_011534289.1:p.Ala327=
XM_011535988.1:c.-20+15736A>C	XP_011534290.1:n.-20+15736A>C
NM_001346813.1:c.2832A>C	NP_001333742.1:p.Ala944=
NM_001363725.1:c.582A>C	NP_001350654.1:p.Ala194=
XM_011535984.2:c.2913A>C	XP_011534286.2:p.Ala971=
XM_011535988.3:c.-20+15736A>C	XP_011534290.1:n.-20+15736A>C
XM_017011103.2:c.2913A>C	XP_016866592.1:p.Ala971=
XM_017011104.1:c.2913A>C	XP_016866593.1:p.Ala971=
XM_017011105.2:c.2913A>C	XP_016866594.1:p.Ala971=
XM_017011106.2:c.2913A>C	XP_016866595.1:p.Ala971=
XM_017011107.2:c.2733A>C	XP_016866596.1:p.Ala911=
XR_002956289.1:n.2996A>C
NM_001363725.2:c.582A>C	NP_001350654.1:p.Ala194=
NM_001371656.1:c.3120A>C	NP_001358585.1:p.Ala1040=
NM_001374820.1:c.3120A>C	NP_001361749.1:p.Ala1040=
NM_001374828.1:c.3081A>C MANE Select	NP_001361757.1:p.Ala1027=
NM_017519.3:c.3081A>C	NP_059989.3:p.Ala1027=