Canonical Allele Identifier: CA366242817

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376395
• MyVariant Identifiers: chr6:g.157522511C>A (hg19) ; chr6:g.157201377C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201377C>A , CM000668.2:g.157201377C>A	GRCh38
NC_000006.11:g.157522511C>A , CM000668.1:g.157522511C>A	GRCh37
NC_000006.10:g.157564203C>A	NCBI36
NG_032093.1:g.428448C>A
NG_032093.2:g.428448C>A
NG_066624.1:g.430352C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4993C>A	ENSP00000055163.8:p.Pro1665Thr
ENST00000414678.8:c.5062C>A	ENSP00000412835.3:p.Pro1688Thr
ENST00000637015.2:c.5281C>A	ENSP00000489729.2:p.Pro1761Thr
ENST00000346085.10:c.5032C>A	ENSP00000344546.5:p.Pro1678Thr
ENST00000350026.10:c.4744C>A	ENSP00000055163.7:p.Pro1582Thr
ENST00000414678.7:c.3310C>A	ENSP00000412835.2:p.Pro1104Thr
ENST00000635849.1:c.2473C>A	ENSP00000490948.1:p.Pro825Thr
ENST00000635957.1:c.2104C>A	ENSP00000490385.1:p.Pro702Thr
ENST00000636227.1:n.3615C>A
ENST00000636254.1:n.1072C>A
ENST00000636930.2:c.5152C>A MANE Select	ENSP00000490491.2:p.Pro1718Thr
ENST00000636940.1:n.3149C>A
ENST00000637015.1:c.2520C>A
ENST00000637568.1:c.2434C>A
ENST00000637741.1:n.1818C>A
ENST00000637810.1:c.2494C>A	ENSP00000489636.1:p.Pro832Thr
ENST00000637904.1:c.2653C>A	ENSP00000490550.1:p.Pro885Thr
ENST00000647938.1:c.4783C>A	ENSP00000498155.1:p.Pro1595Thr
ENST00000346085.9:c.4783C>A	ENSP00000344546.4:p.Pro1595Thr
ENST00000350026.9:c.4744C>A	ENSP00000055163.7:p.Pro1582Thr
ENST00000414678.6:c.3310C>A	ENSP00000412835.2:p.Pro1104Thr
NM_017519.2:c.4744C>A	NP_059989.2:p.Pro1582Thr
NM_020732.3:c.4783C>A	NP_065783.3:p.Pro1595Thr
XM_005267069.3:c.4903C>A	XP_005267126.2:p.Pro1635Thr
XM_011535984.1:c.3982C>A	XP_011534286.1:p.Pro1328Thr
XM_011535985.1:c.3802C>A	XP_011534287.1:p.Pro1268Thr
XM_011535986.1:c.3562C>A	XP_011534288.1:p.Pro1188Thr
XM_011535987.1:c.3181C>A	XP_011534289.1:p.Pro1061Thr
XM_011535988.1:c.2044C>A	XP_011534290.1:p.Pro682Thr
NM_001346813.1:c.4903C>A	NP_001333742.1:p.Pro1635Thr
NM_001363725.1:c.2653C>A	NP_001350654.1:p.Pro885Thr
XM_011535984.2:c.5113C>A	XP_011534286.2:p.Pro1705Thr
XM_011535988.3:c.2044C>A	XP_011534290.1:p.Pro682Thr
XM_017011103.2:c.5014C>A	XP_016866592.1:p.Pro1672Thr
XM_017011104.1:c.4984C>A	XP_016866593.1:p.Pro1662Thr
XM_017011105.2:c.4954C>A	XP_016866594.1:p.Pro1652Thr
XM_017011106.2:c.4825C>A	XP_016866595.1:p.Pro1609Thr
XM_017011107.2:c.4804C>A	XP_016866596.1:p.Pro1602Thr
XR_002956289.1:n.5099C>A
NM_001363725.2:c.2653C>A	NP_001350654.1:p.Pro885Thr
NM_001371656.1:c.5032C>A	NP_001358585.1:p.Pro1678Thr
NM_001374820.1:c.5032C>A	NP_001361749.1:p.Pro1678Thr
NM_001374828.1:c.5152C>A MANE Select	NP_001361757.1:p.Pro1718Thr
NM_017519.3:c.4993C>A	NP_059989.3:p.Pro1665Thr