Canonical Allele Identifier: CA366389207

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554226132
• MyVariant Identifiers: chr6:g.157470036G>T (hg19) ; chr6:g.157148902G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148902G>T , CM000668.2:g.157148902G>T	GRCh38
NC_000006.11:g.157470036G>T , CM000668.1:g.157470036G>T	GRCh37
NC_000006.10:g.157511728G>T	NCBI36
NG_032093.1:g.375973G>T
NG_032093.2:g.375973G>T
NG_066624.1:g.377877G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3040G>T	ENSP00000055163.8:p.Glu1014Ter
ENST00000414678.8:c.2950G>T	ENSP00000412835.3:p.Glu984Ter
ENST00000637015.2:c.3040G>T	ENSP00000489729.2:p.Glu1014Ter
ENST00000319584.11:c.1054G>T	ENSP00000313006.7:p.Glu352Ter
ENST00000346085.10:c.3079G>T	ENSP00000344546.5:p.Glu1027Ter
ENST00000350026.10:c.2791G>T	ENSP00000055163.7:p.Glu931Ter
ENST00000414678.7:c.1198G>T	ENSP00000412835.2:p.Glu400Ter
ENST00000452544.2:n.941G>T
ENST00000635849.1:c.361G>T	ENSP00000490948.1:p.Glu121Ter
ENST00000636426.1:n.174G>T
ENST00000636930.2:c.3040G>T MANE Select	ENSP00000490491.2:p.Glu1014Ter
ENST00000637015.1:c.279G>T
ENST00000637568.1:c.83G>T
ENST00000637810.1:c.541G>T	ENSP00000489636.1:p.Glu181Ter
ENST00000637904.1:c.541G>T	ENSP00000490550.1:p.Glu181Ter
ENST00000647938.1:c.2830G>T	ENSP00000498155.1:p.Glu944Ter
ENST00000674190.1:n.1789G>T
ENST00000319584.10:c.1057G>T	ENSP00000313006.6:p.Glu353Ter
ENST00000346085.9:c.2830G>T	ENSP00000344546.4:p.Glu944Ter
ENST00000350026.9:c.2791G>T	ENSP00000055163.7:p.Glu931Ter
ENST00000414678.6:c.1198G>T	ENSP00000412835.2:p.Glu400Ter
ENST00000452544.1:n.887G>T
ENST00000478761.3:c.113G>T
NM_017519.2:c.2791G>T	NP_059989.2:p.Glu931Ter
NM_020732.3:c.2830G>T	NP_065783.3:p.Glu944Ter
XM_005267069.3:c.2791G>T	XP_005267126.2:p.Glu931Ter
XM_011535984.1:c.1741G>T	XP_011534286.1:p.Glu581Ter
XM_011535985.1:c.1561G>T	XP_011534287.1:p.Glu521Ter
XM_011535986.1:c.1321G>T	XP_011534288.1:p.Glu441Ter
XM_011535987.1:c.940G>T	XP_011534289.1:p.Glu314Ter
XM_011535988.1:c.-20+15695G>T	XP_011534290.1:n.-20+15695G>T
NM_001346813.1:c.2791G>T	NP_001333742.1:p.Glu931Ter
NM_001363725.1:c.541G>T	NP_001350654.1:p.Glu181Ter
XM_011535984.2:c.2872G>T	XP_011534286.2:p.Glu958Ter
XM_011535988.3:c.-20+15695G>T	XP_011534290.1:n.-20+15695G>T
XM_017011103.2:c.2872G>T	XP_016866592.1:p.Glu958Ter
XM_017011104.1:c.2872G>T	XP_016866593.1:p.Glu958Ter
XM_017011105.2:c.2872G>T	XP_016866594.1:p.Glu958Ter
XM_017011106.2:c.2872G>T	XP_016866595.1:p.Glu958Ter
XM_017011107.2:c.2692G>T	XP_016866596.1:p.Glu898Ter
XR_002956289.1:n.2955G>T
NM_001363725.2:c.541G>T	NP_001350654.1:p.Glu181Ter
NM_001371656.1:c.3079G>T	NP_001358585.1:p.Glu1027Ter
NM_001374820.1:c.3079G>T	NP_001361749.1:p.Glu1027Ter
NM_001374828.1:c.3040G>T MANE Select	NP_001361757.1:p.Glu1014Ter
NM_017519.3:c.3040G>T	NP_059989.3:p.Glu1014Ter