Canonical Allele Identifier: CA366241767

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522196T>C (hg19) ; chr6:g.157201062T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201062T>C , CM000668.2:g.157201062T>C	GRCh38
NC_000006.11:g.157522196T>C , CM000668.1:g.157522196T>C	GRCh37
NC_000006.10:g.157563888T>C	NCBI36
NG_032093.1:g.428133T>C
NG_032093.2:g.428133T>C
NG_066624.1:g.430037T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4678T>C	ENSP00000055163.8:p.Tyr1560His
ENST00000414678.8:c.4747T>C	ENSP00000412835.3:p.Tyr1583His
ENST00000637015.2:c.4966T>C	ENSP00000489729.2:p.Tyr1656His
ENST00000346085.10:c.4717T>C	ENSP00000344546.5:p.Tyr1573His
ENST00000350026.10:c.4429T>C	ENSP00000055163.7:p.Tyr1477His
ENST00000414678.7:c.2995T>C	ENSP00000412835.2:p.Tyr999His
ENST00000635849.1:c.2158T>C	ENSP00000490948.1:p.Tyr720His
ENST00000635957.1:c.1789T>C	ENSP00000490385.1:p.Tyr597His
ENST00000636227.1:n.3300T>C
ENST00000636254.1:n.757T>C
ENST00000636930.2:c.4837T>C MANE Select	ENSP00000490491.2:p.Tyr1613His
ENST00000636940.1:n.2834T>C
ENST00000637015.1:c.2205T>C
ENST00000637568.1:c.2119T>C
ENST00000637741.1:n.1503T>C
ENST00000637810.1:c.2179T>C	ENSP00000489636.1:p.Tyr727His
ENST00000637904.1:c.2338T>C	ENSP00000490550.1:p.Tyr780His
ENST00000647938.1:c.4468T>C	ENSP00000498155.1:p.Tyr1490His
ENST00000346085.9:c.4468T>C	ENSP00000344546.4:p.Tyr1490His
ENST00000350026.9:c.4429T>C	ENSP00000055163.7:p.Tyr1477His
ENST00000414678.6:c.2995T>C	ENSP00000412835.2:p.Tyr999His
NM_017519.2:c.4429T>C	NP_059989.2:p.Tyr1477His
NM_020732.3:c.4468T>C	NP_065783.3:p.Tyr1490His
XM_005267069.3:c.4588T>C	XP_005267126.2:p.Tyr1530His
XM_011535984.1:c.3667T>C	XP_011534286.1:p.Tyr1223His
XM_011535985.1:c.3487T>C	XP_011534287.1:p.Tyr1163His
XM_011535986.1:c.3247T>C	XP_011534288.1:p.Tyr1083His
XM_011535987.1:c.2866T>C	XP_011534289.1:p.Tyr956His
XM_011535988.1:c.1729T>C	XP_011534290.1:p.Tyr577His
NM_001346813.1:c.4588T>C	NP_001333742.1:p.Tyr1530His
NM_001363725.1:c.2338T>C	NP_001350654.1:p.Tyr780His
XM_011535984.2:c.4798T>C	XP_011534286.2:p.Tyr1600His
XM_011535988.3:c.1729T>C	XP_011534290.1:p.Tyr577His
XM_017011103.2:c.4699T>C	XP_016866592.1:p.Tyr1567His
XM_017011104.1:c.4669T>C	XP_016866593.1:p.Tyr1557His
XM_017011105.2:c.4639T>C	XP_016866594.1:p.Tyr1547His
XM_017011106.2:c.4510T>C	XP_016866595.1:p.Tyr1504His
XM_017011107.2:c.4489T>C	XP_016866596.1:p.Tyr1497His
XR_002956289.1:n.4784T>C
NM_001363725.2:c.2338T>C	NP_001350654.1:p.Tyr780His
NM_001371656.1:c.4717T>C	NP_001358585.1:p.Tyr1573His
NM_001374820.1:c.4717T>C	NP_001361749.1:p.Tyr1573His
NM_001374828.1:c.4837T>C MANE Select	NP_001361757.1:p.Tyr1613His
NM_017519.3:c.4678T>C	NP_059989.3:p.Tyr1560His