Canonical Allele Identifier: CA366389229

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470046C>A (hg19) ; chr6:g.157148912C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148912C>A , CM000668.2:g.157148912C>A	GRCh38
NC_000006.11:g.157470046C>A , CM000668.1:g.157470046C>A	GRCh37
NC_000006.10:g.157511738C>A	NCBI36
NG_032093.1:g.375983C>A
NG_032093.2:g.375983C>A
NG_066624.1:g.377887C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3050C>A	ENSP00000055163.8:p.Ala1017Glu
ENST00000414678.8:c.2960C>A	ENSP00000412835.3:p.Ala987Glu
ENST00000637015.2:c.3050C>A	ENSP00000489729.2:p.Ala1017Glu
ENST00000319584.11:c.1064C>A	ENSP00000313006.7:p.Ala355Glu
ENST00000346085.10:c.3089C>A	ENSP00000344546.5:p.Ala1030Glu
ENST00000350026.10:c.2801C>A	ENSP00000055163.7:p.Ala934Glu
ENST00000414678.7:c.1208C>A	ENSP00000412835.2:p.Ala403Glu
ENST00000452544.2:n.951C>A
ENST00000635849.1:c.371C>A	ENSP00000490948.1:p.Ala124Glu
ENST00000635957.1:c.5C>A	ENSP00000490385.1:p.Ala2Glu
ENST00000636426.1:n.184C>A
ENST00000636930.2:c.3050C>A MANE Select	ENSP00000490491.2:p.Ala1017Glu
ENST00000637015.1:c.289C>A
ENST00000637568.1:c.93C>A
ENST00000637810.1:c.551C>A	ENSP00000489636.1:p.Ala184Glu
ENST00000637904.1:c.551C>A	ENSP00000490550.1:p.Ala184Glu
ENST00000647938.1:c.2840C>A	ENSP00000498155.1:p.Ala947Glu
ENST00000674190.1:n.1799C>A
ENST00000319584.10:c.1067C>A	ENSP00000313006.6:p.Ala356Glu
ENST00000346085.9:c.2840C>A	ENSP00000344546.4:p.Ala947Glu
ENST00000350026.9:c.2801C>A	ENSP00000055163.7:p.Ala934Glu
ENST00000400790.3:c.2C>A	ENSP00000383596.3:p.Ala1Glu
ENST00000414678.6:c.1208C>A	ENSP00000412835.2:p.Ala403Glu
ENST00000452544.1:n.897C>A
ENST00000478761.3:c.123C>A
NM_017519.2:c.2801C>A	NP_059989.2:p.Ala934Glu
NM_020732.3:c.2840C>A	NP_065783.3:p.Ala947Glu
XM_005267069.3:c.2801C>A	XP_005267126.2:p.Ala934Glu
XM_011535984.1:c.1751C>A	XP_011534286.1:p.Ala584Glu
XM_011535985.1:c.1571C>A	XP_011534287.1:p.Ala524Glu
XM_011535986.1:c.1331C>A	XP_011534288.1:p.Ala444Glu
XM_011535987.1:c.950C>A	XP_011534289.1:p.Ala317Glu
XM_011535988.1:c.-20+15705C>A	XP_011534290.1:n.-20+15705C>A
NM_001346813.1:c.2801C>A	NP_001333742.1:p.Ala934Glu
NM_001363725.1:c.551C>A	NP_001350654.1:p.Ala184Glu
XM_011535984.2:c.2882C>A	XP_011534286.2:p.Ala961Glu
XM_011535988.3:c.-20+15705C>A	XP_011534290.1:n.-20+15705C>A
XM_017011103.2:c.2882C>A	XP_016866592.1:p.Ala961Glu
XM_017011104.1:c.2882C>A	XP_016866593.1:p.Ala961Glu
XM_017011105.2:c.2882C>A	XP_016866594.1:p.Ala961Glu
XM_017011106.2:c.2882C>A	XP_016866595.1:p.Ala961Glu
XM_017011107.2:c.2702C>A	XP_016866596.1:p.Ala901Glu
XR_002956289.1:n.2965C>A
NM_001363725.2:c.551C>A	NP_001350654.1:p.Ala184Glu
NM_001371656.1:c.3089C>A	NP_001358585.1:p.Ala1030Glu
NM_001374820.1:c.3089C>A	NP_001361749.1:p.Ala1030Glu
NM_001374828.1:c.3050C>A MANE Select	NP_001361757.1:p.Ala1017Glu
NM_017519.3:c.3050C>A	NP_059989.3:p.Ala1017Glu