Canonical Allele Identifier: CA366387446

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157406013G>C (hg19) ; chr6:g.157084879G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084879G>C , CM000668.2:g.157084879G>C	GRCh38
NC_000006.11:g.157406013G>C , CM000668.1:g.157406013G>C	GRCh37
NC_000006.10:g.157447705G>C	NCBI36
NG_032093.1:g.311950G>C
NG_032093.2:g.311950G>C
NG_066624.1:g.313854G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2465G>C	ENSP00000055163.8:p.Gly822Ala
ENST00000414678.8:c.2465G>C	ENSP00000412835.3:p.Gly822Ala
ENST00000637015.2:c.2465G>C	ENSP00000489729.2:p.Gly822Ala
ENST00000319584.11:c.479G>C	ENSP00000313006.7:p.Gly160Ala
ENST00000346085.10:c.2504G>C	ENSP00000344546.5:p.Gly835Ala
ENST00000350026.10:c.2216G>C	ENSP00000055163.7:p.Gly739Ala
ENST00000414678.7:c.713G>C	ENSP00000412835.2:p.Gly238Ala
ENST00000452544.2:n.366G>C
ENST00000493658.2:n.114G>C
ENST00000635849.1:c.-35G>C	ENSP00000490948.1:n.-35G>C
ENST00000636930.2:c.2465G>C MANE Select	ENSP00000490491.2:p.Gly822Ala
ENST00000637003.1:c.-35G>C	ENSP00000489666.1:n.-35G>C
ENST00000637810.1:c.-35G>C	ENSP00000489636.1:n.-35G>C
ENST00000637904.1:c.-35G>C	ENSP00000490550.1:n.-35G>C
ENST00000647938.1:c.2255G>C	ENSP00000498155.1:p.Gly752Ala
ENST00000674190.1:n.1214G>C
ENST00000319584.10:c.482G>C	ENSP00000313006.6:p.Gly161Ala
ENST00000346085.9:c.2255G>C	ENSP00000344546.4:p.Gly752Ala
ENST00000350026.9:c.2216G>C	ENSP00000055163.7:p.Gly739Ala
ENST00000414678.6:c.713G>C	ENSP00000412835.2:p.Gly238Ala
ENST00000452544.1:n.324G>C
ENST00000493658.1:n.114G>C
NM_017519.2:c.2216G>C	NP_059989.2:p.Gly739Ala
NM_020732.3:c.2255G>C	NP_065783.3:p.Gly752Ala
XM_005267069.3:c.2216G>C	XP_005267126.2:p.Gly739Ala
XM_011535984.1:c.1166G>C	XP_011534286.1:p.Gly389Ala
XM_011535985.1:c.1166G>C	XP_011534287.1:p.Gly389Ala
XM_011535986.1:c.746G>C	XP_011534288.1:p.Gly249Ala
XM_011535987.1:c.365G>C	XP_011534289.1:p.Gly122Ala
NM_001346813.1:c.2216G>C	NP_001333742.1:p.Gly739Ala
NM_001363725.1:c.-35G>C	NP_001350654.1:n.-35G>C
XM_011535984.2:c.2297G>C	XP_011534286.2:p.Gly766Ala
XM_017011103.2:c.2297G>C	XP_016866592.1:p.Gly766Ala
XM_017011104.1:c.2297G>C	XP_016866593.1:p.Gly766Ala
XM_017011105.2:c.2297G>C	XP_016866594.1:p.Gly766Ala
XM_017011106.2:c.2297G>C	XP_016866595.1:p.Gly766Ala
XM_017011107.2:c.2297G>C	XP_016866596.1:p.Gly766Ala
XR_002956289.1:n.2380G>C
NM_001363725.2:c.-35G>C	NP_001350654.1:n.-35G>C
NM_001371656.1:c.2504G>C	NP_001358585.1:p.Gly835Ala
NM_001374820.1:c.2504G>C	NP_001361749.1:p.Gly835Ala
NM_001374828.1:c.2465G>C MANE Select	NP_001361757.1:p.Gly822Ala
NM_017519.3:c.2465G>C	NP_059989.3:p.Gly822Ala