Canonical Allele Identifier: CA366242822

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4993C>T	ENSP00000055163.8:p.Pro1665Ser
ENST00000414678.8:c.5062C>T	ENSP00000412835.3:p.Pro1688Ser
ENST00000637015.2:c.5281C>T	ENSP00000489729.2:p.Pro1761Ser
ENST00000346085.10:c.5032C>T	ENSP00000344546.5:p.Pro1678Ser
ENST00000350026.10:c.4744C>T	ENSP00000055163.7:p.Pro1582Ser
ENST00000414678.7:c.3310C>T	ENSP00000412835.2:p.Pro1104Ser
ENST00000635849.1:c.2473C>T	ENSP00000490948.1:p.Pro825Ser
ENST00000635957.1:c.2104C>T	ENSP00000490385.1:p.Pro702Ser
ENST00000636227.1:n.3615C>T
ENST00000636254.1:n.1072C>T
ENST00000636930.2:c.5152C>T MANE Select	ENSP00000490491.2:p.Pro1718Ser
ENST00000636940.1:n.3149C>T
ENST00000637015.1:c.2520C>T
ENST00000637568.1:c.2434C>T
ENST00000637741.1:n.1818C>T
ENST00000637810.1:c.2494C>T	ENSP00000489636.1:p.Pro832Ser
ENST00000637904.1:c.2653C>T	ENSP00000490550.1:p.Pro885Ser
ENST00000647938.1:c.4783C>T	ENSP00000498155.1:p.Pro1595Ser
ENST00000346085.9:c.4783C>T	ENSP00000344546.4:p.Pro1595Ser
ENST00000350026.9:c.4744C>T	ENSP00000055163.7:p.Pro1582Ser
ENST00000414678.6:c.3310C>T	ENSP00000412835.2:p.Pro1104Ser
NM_017519.2:c.4744C>T	NP_059989.2:p.Pro1582Ser
NM_020732.3:c.4783C>T	NP_065783.3:p.Pro1595Ser
XM_005267069.3:c.4903C>T	XP_005267126.2:p.Pro1635Ser
XM_011535984.1:c.3982C>T	XP_011534286.1:p.Pro1328Ser
XM_011535985.1:c.3802C>T	XP_011534287.1:p.Pro1268Ser
XM_011535986.1:c.3562C>T	XP_011534288.1:p.Pro1188Ser
XM_011535987.1:c.3181C>T	XP_011534289.1:p.Pro1061Ser
XM_011535988.1:c.2044C>T	XP_011534290.1:p.Pro682Ser
NM_001346813.1:c.4903C>T	NP_001333742.1:p.Pro1635Ser
NM_001363725.1:c.2653C>T	NP_001350654.1:p.Pro885Ser
XM_011535984.2:c.5113C>T	XP_011534286.2:p.Pro1705Ser
XM_011535988.3:c.2044C>T	XP_011534290.1:p.Pro682Ser
XM_017011103.2:c.5014C>T	XP_016866592.1:p.Pro1672Ser
XM_017011104.1:c.4984C>T	XP_016866593.1:p.Pro1662Ser
XM_017011105.2:c.4954C>T	XP_016866594.1:p.Pro1652Ser
XM_017011106.2:c.4825C>T	XP_016866595.1:p.Pro1609Ser
XM_017011107.2:c.4804C>T	XP_016866596.1:p.Pro1602Ser
XR_002956289.1:n.5099C>T
NM_001363725.2:c.2653C>T	NP_001350654.1:p.Pro885Ser
NM_001371656.1:c.5032C>T	NP_001358585.1:p.Pro1678Ser
NM_001374820.1:c.5032C>T	NP_001361749.1:p.Pro1678Ser
NM_001374828.1:c.5152C>T MANE Select	NP_001361757.1:p.Pro1718Ser
NM_017519.3:c.4993C>T	NP_059989.3:p.Pro1665Ser