Canonical Allele Identifier: CA366389114

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469992C>A (hg19) ; chr6:g.157148858C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148858C>A , CM000668.2:g.157148858C>A	GRCh38
NC_000006.11:g.157469992C>A , CM000668.1:g.157469992C>A	GRCh37
NC_000006.10:g.157511684C>A	NCBI36
NG_032093.1:g.375929C>A
NG_032093.2:g.375929C>A
NG_066624.1:g.377833C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.2996C>A	ENSP00000055163.8:p.Pro999Gln
ENST00000414678.8:c.2906C>A	ENSP00000412835.3:p.Pro969Gln
ENST00000637015.2:c.2996C>A	ENSP00000489729.2:p.Pro999Gln
ENST00000319584.11:c.1010C>A	ENSP00000313006.7:p.Pro337Gln
ENST00000346085.10:c.3035C>A	ENSP00000344546.5:p.Pro1012Gln
ENST00000350026.10:c.2747C>A	ENSP00000055163.7:p.Pro916Gln
ENST00000414678.7:c.1154C>A	ENSP00000412835.2:p.Pro385Gln
ENST00000452544.2:n.897C>A
ENST00000635849.1:c.317C>A	ENSP00000490948.1:p.Pro106Gln
ENST00000636426.1:n.130C>A
ENST00000636930.2:c.2996C>A MANE Select	ENSP00000490491.2:p.Pro999Gln
ENST00000637015.1:c.235C>A
ENST00000637568.1:c.39C>A
ENST00000637810.1:c.497C>A	ENSP00000489636.1:p.Pro166Gln
ENST00000637904.1:c.497C>A	ENSP00000490550.1:p.Pro166Gln
ENST00000647938.1:c.2786C>A	ENSP00000498155.1:p.Pro929Gln
ENST00000674190.1:n.1745C>A
ENST00000319584.10:c.1013C>A	ENSP00000313006.6:p.Pro338Gln
ENST00000346085.9:c.2786C>A	ENSP00000344546.4:p.Pro929Gln
ENST00000350026.9:c.2747C>A	ENSP00000055163.7:p.Pro916Gln
ENST00000414678.6:c.1154C>A	ENSP00000412835.2:p.Pro385Gln
ENST00000452544.1:n.843C>A
ENST00000478761.3:c.69C>A
NM_017519.2:c.2747C>A	NP_059989.2:p.Pro916Gln
NM_020732.3:c.2786C>A	NP_065783.3:p.Pro929Gln
XM_005267069.3:c.2747C>A	XP_005267126.2:p.Pro916Gln
XM_011535984.1:c.1697C>A	XP_011534286.1:p.Pro566Gln
XM_011535985.1:c.1517C>A	XP_011534287.1:p.Pro506Gln
XM_011535986.1:c.1277C>A	XP_011534288.1:p.Pro426Gln
XM_011535987.1:c.896C>A	XP_011534289.1:p.Pro299Gln
XM_011535988.1:c.-20+15651C>A	XP_011534290.1:n.-20+15651C>A
NM_001346813.1:c.2747C>A	NP_001333742.1:p.Pro916Gln
NM_001363725.1:c.497C>A	NP_001350654.1:p.Pro166Gln
XM_011535984.2:c.2828C>A	XP_011534286.2:p.Pro943Gln
XM_011535988.3:c.-20+15651C>A	XP_011534290.1:n.-20+15651C>A
XM_017011103.2:c.2828C>A	XP_016866592.1:p.Pro943Gln
XM_017011104.1:c.2828C>A	XP_016866593.1:p.Pro943Gln
XM_017011105.2:c.2828C>A	XP_016866594.1:p.Pro943Gln
XM_017011106.2:c.2828C>A	XP_016866595.1:p.Pro943Gln
XM_017011107.2:c.2648C>A	XP_016866596.1:p.Pro883Gln
XR_002956289.1:n.2911C>A
NM_001363725.2:c.497C>A	NP_001350654.1:p.Pro166Gln
NM_001371656.1:c.3035C>A	NP_001358585.1:p.Pro1012Gln
NM_001374820.1:c.3035C>A	NP_001361749.1:p.Pro1012Gln
NM_001374828.1:c.2996C>A MANE Select	NP_001361757.1:p.Pro999Gln
NM_017519.3:c.2996C>A	NP_059989.3:p.Pro999Gln