Canonical Allele Identifier: CA452989975

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469759T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148625T>C , CM000668.2:g.157148625T>C	GRCh38
NC_000006.11:g.157469759T>C , CM000668.1:g.157469759T>C	GRCh37
NC_000006.10:g.157511451T>C	NCBI36
NG_032093.1:g.375696T>C
NG_032093.2:g.375696T>C
NG_066624.1:g.377600T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2763T>C	ENSP00000055163.8:p.Gly921=
ENST00000414678.8:c.2673T>C	ENSP00000412835.3:p.Gly891=
ENST00000637015.2:c.2763T>C	ENSP00000489729.2:p.Gly921=
ENST00000319584.11:c.777T>C	ENSP00000313006.7:p.Gly259=
ENST00000346085.10:c.2802T>C	ENSP00000344546.5:p.Gly934=
ENST00000350026.10:c.2514T>C	ENSP00000055163.7:p.Gly838=
ENST00000414678.7:c.921T>C	ENSP00000412835.2:p.Gly307=
ENST00000452544.2:n.664T>C
ENST00000635849.1:c.84T>C	ENSP00000490948.1:p.Gly28=
ENST00000636930.2:c.2763T>C MANE Select	ENSP00000490491.2:p.Gly921=
ENST00000637015.1:c.2T>C
ENST00000637810.1:c.264T>C	ENSP00000489636.1:p.Gly88=
ENST00000637904.1:c.264T>C	ENSP00000490550.1:p.Gly88=
ENST00000647938.1:c.2553T>C	ENSP00000498155.1:p.Gly851=
ENST00000674190.1:n.1512T>C
ENST00000319584.10:c.780T>C	ENSP00000313006.6:p.Gly260=
ENST00000346085.9:c.2553T>C	ENSP00000344546.4:p.Gly851=
ENST00000350026.9:c.2514T>C	ENSP00000055163.7:p.Gly838=
ENST00000414678.6:c.921T>C	ENSP00000412835.2:p.Gly307=
ENST00000452544.1:n.610T>C
NM_017519.2:c.2514T>C	NP_059989.2:p.Gly838=
NM_020732.3:c.2553T>C	NP_065783.3:p.Gly851=
XM_005267069.3:c.2514T>C	XP_005267126.2:p.Gly838=
XM_011535984.1:c.1464T>C	XP_011534286.1:p.Gly488=
XM_011535985.1:c.1284T>C	XP_011534287.1:p.Gly428=
XM_011535986.1:c.1044T>C	XP_011534288.1:p.Gly348=
XM_011535987.1:c.663T>C	XP_011534289.1:p.Gly221=
XM_011535988.1:c.-20+15418T>C	XP_011534290.1:n.-20+15418T>C
NM_001346813.1:c.2514T>C	NP_001333742.1:p.Gly838=
NM_001363725.1:c.264T>C	NP_001350654.1:p.Gly88=
XM_011535984.2:c.2595T>C	XP_011534286.2:p.Gly865=
XM_011535988.3:c.-20+15418T>C	XP_011534290.1:n.-20+15418T>C
XM_017011103.2:c.2595T>C	XP_016866592.1:p.Gly865=
XM_017011104.1:c.2595T>C	XP_016866593.1:p.Gly865=
XM_017011105.2:c.2595T>C	XP_016866594.1:p.Gly865=
XM_017011106.2:c.2595T>C	XP_016866595.1:p.Gly865=
XM_017011107.2:c.2415T>C	XP_016866596.1:p.Gly805=
XR_002956289.1:n.2678T>C
NM_001363725.2:c.264T>C	NP_001350654.1:p.Gly88=
NM_001371656.1:c.2802T>C	NP_001358585.1:p.Gly934=
NM_001374820.1:c.2802T>C	NP_001361749.1:p.Gly934=
NM_001374828.1:c.2763T>C MANE Select	NP_001361757.1:p.Gly921=
NM_017519.3:c.2763T>C	NP_059989.3:p.Gly921=