Canonical Allele Identifier: CA366249637

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207818C>T , CM000668.2:g.157207818C>T	GRCh38
NC_000006.11:g.157528952C>T , CM000668.1:g.157528952C>T	GRCh37
NC_000006.10:g.157570644C>T	NCBI36
NG_032093.1:g.434889C>T
NG_032093.2:g.434889C>T
NG_066624.1:g.436793C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.6887C>T	ENSP00000055163.8:p.Ser2296Leu
ENST00000414678.8:c.6956C>T	ENSP00000412835.3:p.Ser2319Leu
ENST00000637015.2:c.7175C>T	ENSP00000489729.2:p.Ser2392Leu
ENST00000346085.10:c.6926C>T	ENSP00000344546.5:p.Ser2309Leu
ENST00000350026.10:c.6638C>T	ENSP00000055163.7:p.Ser2213Leu
ENST00000414678.7:c.5204C>T	ENSP00000412835.2:p.Ser1735Leu
ENST00000635849.1:c.4367C>T	ENSP00000490948.1:p.Ser1456Leu
ENST00000635928.1:c.875+327C>T	ENSP00000489717.1:n.875+327C>T
ENST00000635957.1:c.3998C>T	ENSP00000490385.1:p.Ser1333Leu
ENST00000636227.1:n.5509C>T
ENST00000636254.1:n.2966C>T
ENST00000636930.2:c.7046C>T MANE Select	ENSP00000490491.2:p.Ser2349Leu
ENST00000636940.1:n.5043C>T
ENST00000637015.1:c.4414C>T
ENST00000637568.1:c.4328C>T
ENST00000637741.1:n.3712C>T
ENST00000637810.1:c.4388C>T	ENSP00000489636.1:p.Ser1463Leu
ENST00000637904.1:c.4547C>T	ENSP00000490550.1:p.Ser1516Leu
ENST00000637933.1:n.4161C>T
ENST00000647938.1:c.6677C>T	ENSP00000498155.1:p.Ser2226Leu
ENST00000346085.9:c.6677C>T	ENSP00000344546.4:p.Ser2226Leu
ENST00000350026.9:c.6638C>T	ENSP00000055163.7:p.Ser2213Leu
ENST00000414678.6:c.5204C>T	ENSP00000412835.2:p.Ser1735Leu
NM_017519.2:c.6638C>T	NP_059989.2:p.Ser2213Leu
NM_020732.3:c.6677C>T	NP_065783.3:p.Ser2226Leu
XM_005267069.3:c.6797C>T	XP_005267126.2:p.Ser2266Leu
XM_011535984.1:c.5876C>T	XP_011534286.1:p.Ser1959Leu
XM_011535985.1:c.5696C>T	XP_011534287.1:p.Ser1899Leu
XM_011535986.1:c.5456C>T	XP_011534288.1:p.Ser1819Leu
XM_011535987.1:c.5075C>T	XP_011534289.1:p.Ser1692Leu
XM_011535988.1:c.3938C>T	XP_011534290.1:p.Ser1313Leu
NM_001346813.1:c.6797C>T	NP_001333742.1:p.Ser2266Leu
NM_001363725.1:c.4547C>T	NP_001350654.1:p.Ser1516Leu
XM_011535984.2:c.7007C>T	XP_011534286.2:p.Ser2336Leu
XM_011535988.3:c.3938C>T	XP_011534290.1:p.Ser1313Leu
XM_017011103.2:c.6908C>T	XP_016866592.1:p.Ser2303Leu
XM_017011104.1:c.6878C>T	XP_016866593.1:p.Ser2293Leu
XM_017011105.2:c.6848C>T	XP_016866594.1:p.Ser2283Leu
XM_017011106.2:c.6719C>T	XP_016866595.1:p.Ser2240Leu
XM_017011107.2:c.6698C>T	XP_016866596.1:p.Ser2233Leu
XR_002956289.1:n.6993C>T
NM_001363725.2:c.4547C>T	NP_001350654.1:p.Ser1516Leu
NM_001371656.1:c.6926C>T	NP_001358585.1:p.Ser2309Leu
NM_001374820.1:c.6926C>T	NP_001361749.1:p.Ser2309Leu
NM_001374828.1:c.7046C>T MANE Select	NP_001361757.1:p.Ser2349Leu
NM_017519.3:c.6887C>T	NP_059989.3:p.Ser2296Leu