Canonical Allele Identifier: CA452990220

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469939A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148805A>C , CM000668.2:g.157148805A>C	GRCh38
NC_000006.11:g.157469939A>C , CM000668.1:g.157469939A>C	GRCh37
NC_000006.10:g.157511631A>C	NCBI36
NG_032093.1:g.375876A>C
NG_032093.2:g.375876A>C
NG_066624.1:g.377780A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2943A>C	ENSP00000055163.8:p.Gly981=
ENST00000414678.8:c.2853A>C	ENSP00000412835.3:p.Gly951=
ENST00000637015.2:c.2943A>C	ENSP00000489729.2:p.Gly981=
ENST00000319584.11:c.957A>C	ENSP00000313006.7:p.Gly319=
ENST00000346085.10:c.2982A>C	ENSP00000344546.5:p.Gly994=
ENST00000350026.10:c.2694A>C	ENSP00000055163.7:p.Gly898=
ENST00000414678.7:c.1101A>C	ENSP00000412835.2:p.Gly367=
ENST00000452544.2:n.844A>C
ENST00000635849.1:c.264A>C	ENSP00000490948.1:p.Gly88=
ENST00000636426.1:n.77A>C
ENST00000636930.2:c.2943A>C MANE Select	ENSP00000490491.2:p.Gly981=
ENST00000637015.1:c.182A>C
ENST00000637810.1:c.444A>C	ENSP00000489636.1:p.Gly148=
ENST00000637904.1:c.444A>C	ENSP00000490550.1:p.Gly148=
ENST00000647938.1:c.2733A>C	ENSP00000498155.1:p.Gly911=
ENST00000674190.1:n.1692A>C
ENST00000319584.10:c.960A>C	ENSP00000313006.6:p.Gly320=
ENST00000346085.9:c.2733A>C	ENSP00000344546.4:p.Gly911=
ENST00000350026.9:c.2694A>C	ENSP00000055163.7:p.Gly898=
ENST00000414678.6:c.1101A>C	ENSP00000412835.2:p.Gly367=
ENST00000452544.1:n.790A>C
ENST00000478761.3:c.16A>C
NM_017519.2:c.2694A>C	NP_059989.2:p.Gly898=
NM_020732.3:c.2733A>C	NP_065783.3:p.Gly911=
XM_005267069.3:c.2694A>C	XP_005267126.2:p.Gly898=
XM_011535984.1:c.1644A>C	XP_011534286.1:p.Gly548=
XM_011535985.1:c.1464A>C	XP_011534287.1:p.Gly488=
XM_011535986.1:c.1224A>C	XP_011534288.1:p.Gly408=
XM_011535987.1:c.843A>C	XP_011534289.1:p.Gly281=
XM_011535988.1:c.-20+15598A>C	XP_011534290.1:n.-20+15598A>C
NM_001346813.1:c.2694A>C	NP_001333742.1:p.Gly898=
NM_001363725.1:c.444A>C	NP_001350654.1:p.Gly148=
XM_011535984.2:c.2775A>C	XP_011534286.2:p.Gly925=
XM_011535988.3:c.-20+15598A>C	XP_011534290.1:n.-20+15598A>C
XM_017011103.2:c.2775A>C	XP_016866592.1:p.Gly925=
XM_017011104.1:c.2775A>C	XP_016866593.1:p.Gly925=
XM_017011105.2:c.2775A>C	XP_016866594.1:p.Gly925=
XM_017011106.2:c.2775A>C	XP_016866595.1:p.Gly925=
XM_017011107.2:c.2595A>C	XP_016866596.1:p.Gly865=
XR_002956289.1:n.2858A>C
NM_001363725.2:c.444A>C	NP_001350654.1:p.Gly148=
NM_001371656.1:c.2982A>C	NP_001358585.1:p.Gly994=
NM_001374820.1:c.2982A>C	NP_001361749.1:p.Gly994=
NM_001374828.1:c.2943A>C MANE Select	NP_001361757.1:p.Gly981=
NM_017519.3:c.2943A>C	NP_059989.3:p.Gly981=