Canonical Allele Identifier: CA366389268

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128635006
• MyVariant Identifiers: chr6:g.157470064C>T (hg19) ; chr6:g.157148930C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148930C>T , CM000668.2:g.157148930C>T	GRCh38
NC_000006.11:g.157470064C>T , CM000668.1:g.157470064C>T	GRCh37
NC_000006.10:g.157511756C>T	NCBI36
NG_032093.1:g.376001C>T
NG_032093.2:g.376001C>T
NG_066624.1:g.377905C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3068C>T	ENSP00000055163.8:p.Ala1023Val
ENST00000414678.8:c.2978C>T	ENSP00000412835.3:p.Ala993Val
ENST00000637015.2:c.3068C>T	ENSP00000489729.2:p.Ala1023Val
ENST00000319584.11:c.1082C>T	ENSP00000313006.7:p.Ala361Val
ENST00000346085.10:c.3107C>T	ENSP00000344546.5:p.Ala1036Val
ENST00000350026.10:c.2819C>T	ENSP00000055163.7:p.Ala940Val
ENST00000414678.7:c.1226C>T	ENSP00000412835.2:p.Ala409Val
ENST00000452544.2:n.969C>T
ENST00000635849.1:c.389C>T	ENSP00000490948.1:p.Ala130Val
ENST00000635957.1:c.23C>T	ENSP00000490385.1:p.Ala8Val
ENST00000636426.1:n.202C>T
ENST00000636930.2:c.3068C>T MANE Select	ENSP00000490491.2:p.Ala1023Val
ENST00000637015.1:c.307C>T
ENST00000637568.1:c.111C>T
ENST00000637810.1:c.569C>T	ENSP00000489636.1:p.Ala190Val
ENST00000637904.1:c.569C>T	ENSP00000490550.1:p.Ala190Val
ENST00000647938.1:c.2858C>T	ENSP00000498155.1:p.Ala953Val
ENST00000674190.1:n.1817C>T
ENST00000319584.10:c.1085C>T	ENSP00000313006.6:p.Ala362Val
ENST00000346085.9:c.2858C>T	ENSP00000344546.4:p.Ala953Val
ENST00000350026.9:c.2819C>T	ENSP00000055163.7:p.Ala940Val
ENST00000400790.3:c.20C>T	ENSP00000383596.3:p.Ala7Val
ENST00000414678.6:c.1226C>T	ENSP00000412835.2:p.Ala409Val
ENST00000452544.1:n.915C>T
ENST00000478761.3:c.141C>T
NM_017519.2:c.2819C>T	NP_059989.2:p.Ala940Val
NM_020732.3:c.2858C>T	NP_065783.3:p.Ala953Val
XM_005267069.3:c.2819C>T	XP_005267126.2:p.Ala940Val
XM_011535984.1:c.1769C>T	XP_011534286.1:p.Ala590Val
XM_011535985.1:c.1589C>T	XP_011534287.1:p.Ala530Val
XM_011535986.1:c.1349C>T	XP_011534288.1:p.Ala450Val
XM_011535987.1:c.968C>T	XP_011534289.1:p.Ala323Val
XM_011535988.1:c.-20+15723C>T	XP_011534290.1:n.-20+15723C>T
NM_001346813.1:c.2819C>T	NP_001333742.1:p.Ala940Val
NM_001363725.1:c.569C>T	NP_001350654.1:p.Ala190Val
XM_011535984.2:c.2900C>T	XP_011534286.2:p.Ala967Val
XM_011535988.3:c.-20+15723C>T	XP_011534290.1:n.-20+15723C>T
XM_017011103.2:c.2900C>T	XP_016866592.1:p.Ala967Val
XM_017011104.1:c.2900C>T	XP_016866593.1:p.Ala967Val
XM_017011105.2:c.2900C>T	XP_016866594.1:p.Ala967Val
XM_017011106.2:c.2900C>T	XP_016866595.1:p.Ala967Val
XM_017011107.2:c.2720C>T	XP_016866596.1:p.Ala907Val
XR_002956289.1:n.2983C>T
NM_001363725.2:c.569C>T	NP_001350654.1:p.Ala190Val
NM_001371656.1:c.3107C>T	NP_001358585.1:p.Ala1036Val
NM_001374820.1:c.3107C>T	NP_001361749.1:p.Ala1036Val
NM_001374828.1:c.3068C>T MANE Select	NP_001361757.1:p.Ala1023Val
NM_017519.3:c.3068C>T	NP_059989.3:p.Ala1023Val