Canonical Allele Identifier: CA452978069

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522099T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200965T>C , CM000668.2:g.157200965T>C	GRCh38
NC_000006.11:g.157522099T>C , CM000668.1:g.157522099T>C	GRCh37
NC_000006.10:g.157563791T>C	NCBI36
NG_032093.1:g.428036T>C
NG_032093.2:g.428036T>C
NG_066624.1:g.429940T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4581T>C	ENSP00000055163.8:p.Ser1527=
ENST00000414678.8:c.4650T>C	ENSP00000412835.3:p.Ser1550=
ENST00000637015.2:c.4869T>C	ENSP00000489729.2:p.Ser1623=
ENST00000346085.10:c.4620T>C	ENSP00000344546.5:p.Ser1540=
ENST00000350026.10:c.4332T>C	ENSP00000055163.7:p.Ser1444=
ENST00000414678.7:c.2898T>C	ENSP00000412835.2:p.Ser966=
ENST00000635849.1:c.2061T>C	ENSP00000490948.1:p.Ser687=
ENST00000635957.1:c.1692T>C	ENSP00000490385.1:p.Ser564=
ENST00000636227.1:n.3203T>C
ENST00000636254.1:n.660T>C
ENST00000636930.2:c.4740T>C MANE Select	ENSP00000490491.2:p.Ser1580=
ENST00000636940.1:n.2737T>C
ENST00000637015.1:c.2108T>C
ENST00000637568.1:c.2022T>C
ENST00000637741.1:n.1406T>C
ENST00000637810.1:c.2082T>C	ENSP00000489636.1:p.Ser694=
ENST00000637904.1:c.2241T>C	ENSP00000490550.1:p.Ser747=
ENST00000647938.1:c.4371T>C	ENSP00000498155.1:p.Ser1457=
ENST00000346085.9:c.4371T>C	ENSP00000344546.4:p.Ser1457=
ENST00000350026.9:c.4332T>C	ENSP00000055163.7:p.Ser1444=
ENST00000414678.6:c.2898T>C	ENSP00000412835.2:p.Ser966=
NM_017519.2:c.4332T>C	NP_059989.2:p.Ser1444=
NM_020732.3:c.4371T>C	NP_065783.3:p.Ser1457=
XM_005267069.3:c.4491T>C	XP_005267126.2:p.Ser1497=
XM_011535984.1:c.3570T>C	XP_011534286.1:p.Ser1190=
XM_011535985.1:c.3390T>C	XP_011534287.1:p.Ser1130=
XM_011535986.1:c.3150T>C	XP_011534288.1:p.Ser1050=
XM_011535987.1:c.2769T>C	XP_011534289.1:p.Ser923=
XM_011535988.1:c.1632T>C	XP_011534290.1:p.Ser544=
NM_001346813.1:c.4491T>C	NP_001333742.1:p.Ser1497=
NM_001363725.1:c.2241T>C	NP_001350654.1:p.Ser747=
XM_011535984.2:c.4701T>C	XP_011534286.2:p.Ser1567=
XM_011535988.3:c.1632T>C	XP_011534290.1:p.Ser544=
XM_017011103.2:c.4602T>C	XP_016866592.1:p.Ser1534=
XM_017011104.1:c.4572T>C	XP_016866593.1:p.Ser1524=
XM_017011105.2:c.4542T>C	XP_016866594.1:p.Ser1514=
XM_017011106.2:c.4413T>C	XP_016866595.1:p.Ser1471=
XM_017011107.2:c.4392T>C	XP_016866596.1:p.Ser1464=
XR_002956289.1:n.4687T>C
NM_001363725.2:c.2241T>C	NP_001350654.1:p.Ser747=
NM_001371656.1:c.4620T>C	NP_001358585.1:p.Ser1540=
NM_001374820.1:c.4620T>C	NP_001361749.1:p.Ser1540=
NM_001374828.1:c.4740T>C MANE Select	NP_001361757.1:p.Ser1580=
NM_017519.3:c.4581T>C	NP_059989.3:p.Ser1527=