Canonical Allele Identifier: CA452989986

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469769A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148635A>C , CM000668.2:g.157148635A>C	GRCh38
NC_000006.11:g.157469769A>C , CM000668.1:g.157469769A>C	GRCh37
NC_000006.10:g.157511461A>C	NCBI36
NG_032093.1:g.375706A>C
NG_032093.2:g.375706A>C
NG_066624.1:g.377610A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2773A>C	ENSP00000055163.8:p.Arg925=
ENST00000414678.8:c.2683A>C	ENSP00000412835.3:p.Arg895=
ENST00000637015.2:c.2773A>C	ENSP00000489729.2:p.Arg925=
ENST00000319584.11:c.787A>C	ENSP00000313006.7:p.Arg263=
ENST00000346085.10:c.2812A>C	ENSP00000344546.5:p.Arg938=
ENST00000350026.10:c.2524A>C	ENSP00000055163.7:p.Arg842=
ENST00000414678.7:c.931A>C	ENSP00000412835.2:p.Arg311=
ENST00000452544.2:n.674A>C
ENST00000635849.1:c.94A>C	ENSP00000490948.1:p.Arg32=
ENST00000636930.2:c.2773A>C MANE Select	ENSP00000490491.2:p.Arg925=
ENST00000637015.1:c.12A>C
ENST00000637810.1:c.274A>C	ENSP00000489636.1:p.Arg92=
ENST00000637904.1:c.274A>C	ENSP00000490550.1:p.Arg92=
ENST00000647938.1:c.2563A>C	ENSP00000498155.1:p.Arg855=
ENST00000674190.1:n.1522A>C
ENST00000319584.10:c.790A>C	ENSP00000313006.6:p.Arg264=
ENST00000346085.9:c.2563A>C	ENSP00000344546.4:p.Arg855=
ENST00000350026.9:c.2524A>C	ENSP00000055163.7:p.Arg842=
ENST00000414678.6:c.931A>C	ENSP00000412835.2:p.Arg311=
ENST00000452544.1:n.620A>C
NM_017519.2:c.2524A>C	NP_059989.2:p.Arg842=
NM_020732.3:c.2563A>C	NP_065783.3:p.Arg855=
XM_005267069.3:c.2524A>C	XP_005267126.2:p.Arg842=
XM_011535984.1:c.1474A>C	XP_011534286.1:p.Arg492=
XM_011535985.1:c.1294A>C	XP_011534287.1:p.Arg432=
XM_011535986.1:c.1054A>C	XP_011534288.1:p.Arg352=
XM_011535987.1:c.673A>C	XP_011534289.1:p.Arg225=
XM_011535988.1:c.-20+15428A>C	XP_011534290.1:n.-20+15428A>C
NM_001346813.1:c.2524A>C	NP_001333742.1:p.Arg842=
NM_001363725.1:c.274A>C	NP_001350654.1:p.Arg92=
XM_011535984.2:c.2605A>C	XP_011534286.2:p.Arg869=
XM_011535988.3:c.-20+15428A>C	XP_011534290.1:n.-20+15428A>C
XM_017011103.2:c.2605A>C	XP_016866592.1:p.Arg869=
XM_017011104.1:c.2605A>C	XP_016866593.1:p.Arg869=
XM_017011105.2:c.2605A>C	XP_016866594.1:p.Arg869=
XM_017011106.2:c.2605A>C	XP_016866595.1:p.Arg869=
XM_017011107.2:c.2425A>C	XP_016866596.1:p.Arg809=
XR_002956289.1:n.2688A>C
NM_001363725.2:c.274A>C	NP_001350654.1:p.Arg92=
NM_001371656.1:c.2812A>C	NP_001358585.1:p.Arg938=
NM_001374820.1:c.2812A>C	NP_001361749.1:p.Arg938=
NM_001374828.1:c.2773A>C MANE Select	NP_001361757.1:p.Arg925=
NM_017519.3:c.2773A>C	NP_059989.3:p.Arg925=