Canonical Allele Identifier: CA366241664

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522175G>C (hg19) ; chr6:g.157201041G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201041G>C , CM000668.2:g.157201041G>C	GRCh38
NC_000006.11:g.157522175G>C , CM000668.1:g.157522175G>C	GRCh37
NC_000006.10:g.157563867G>C	NCBI36
NG_032093.1:g.428112G>C
NG_032093.2:g.428112G>C
NG_066624.1:g.430016G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4657G>C	ENSP00000055163.8:p.Gly1553Arg
ENST00000414678.8:c.4726G>C	ENSP00000412835.3:p.Gly1576Arg
ENST00000637015.2:c.4945G>C	ENSP00000489729.2:p.Gly1649Arg
ENST00000346085.10:c.4696G>C	ENSP00000344546.5:p.Gly1566Arg
ENST00000350026.10:c.4408G>C	ENSP00000055163.7:p.Gly1470Arg
ENST00000414678.7:c.2974G>C	ENSP00000412835.2:p.Gly992Arg
ENST00000635849.1:c.2137G>C	ENSP00000490948.1:p.Gly713Arg
ENST00000635957.1:c.1768G>C	ENSP00000490385.1:p.Gly590Arg
ENST00000636227.1:n.3279G>C
ENST00000636254.1:n.736G>C
ENST00000636930.2:c.4816G>C MANE Select	ENSP00000490491.2:p.Gly1606Arg
ENST00000636940.1:n.2813G>C
ENST00000637015.1:c.2184G>C
ENST00000637568.1:c.2098G>C
ENST00000637741.1:n.1482G>C
ENST00000637810.1:c.2158G>C	ENSP00000489636.1:p.Gly720Arg
ENST00000637904.1:c.2317G>C	ENSP00000490550.1:p.Gly773Arg
ENST00000647938.1:c.4447G>C	ENSP00000498155.1:p.Gly1483Arg
ENST00000346085.9:c.4447G>C	ENSP00000344546.4:p.Gly1483Arg
ENST00000350026.9:c.4408G>C	ENSP00000055163.7:p.Gly1470Arg
ENST00000414678.6:c.2974G>C	ENSP00000412835.2:p.Gly992Arg
NM_017519.2:c.4408G>C	NP_059989.2:p.Gly1470Arg
NM_020732.3:c.4447G>C	NP_065783.3:p.Gly1483Arg
XM_005267069.3:c.4567G>C	XP_005267126.2:p.Gly1523Arg
XM_011535984.1:c.3646G>C	XP_011534286.1:p.Gly1216Arg
XM_011535985.1:c.3466G>C	XP_011534287.1:p.Gly1156Arg
XM_011535986.1:c.3226G>C	XP_011534288.1:p.Gly1076Arg
XM_011535987.1:c.2845G>C	XP_011534289.1:p.Gly949Arg
XM_011535988.1:c.1708G>C	XP_011534290.1:p.Gly570Arg
NM_001346813.1:c.4567G>C	NP_001333742.1:p.Gly1523Arg
NM_001363725.1:c.2317G>C	NP_001350654.1:p.Gly773Arg
XM_011535984.2:c.4777G>C	XP_011534286.2:p.Gly1593Arg
XM_011535988.3:c.1708G>C	XP_011534290.1:p.Gly570Arg
XM_017011103.2:c.4678G>C	XP_016866592.1:p.Gly1560Arg
XM_017011104.1:c.4648G>C	XP_016866593.1:p.Gly1550Arg
XM_017011105.2:c.4618G>C	XP_016866594.1:p.Gly1540Arg
XM_017011106.2:c.4489G>C	XP_016866595.1:p.Gly1497Arg
XM_017011107.2:c.4468G>C	XP_016866596.1:p.Gly1490Arg
XR_002956289.1:n.4763G>C
NM_001363725.2:c.2317G>C	NP_001350654.1:p.Gly773Arg
NM_001371656.1:c.4696G>C	NP_001358585.1:p.Gly1566Arg
NM_001374820.1:c.4696G>C	NP_001361749.1:p.Gly1566Arg
NM_001374828.1:c.4816G>C MANE Select	NP_001361757.1:p.Gly1606Arg
NM_017519.3:c.4657G>C	NP_059989.3:p.Gly1553Arg