Canonical Allele Identifier: CA366389110

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469991C>A (hg19) ; chr6:g.157148857C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148857C>A , CM000668.2:g.157148857C>A	GRCh38
NC_000006.11:g.157469991C>A , CM000668.1:g.157469991C>A	GRCh37
NC_000006.10:g.157511683C>A	NCBI36
NG_032093.1:g.375928C>A
NG_032093.2:g.375928C>A
NG_066624.1:g.377832C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2995C>A	ENSP00000055163.8:p.Pro999Thr
ENST00000414678.8:c.2905C>A	ENSP00000412835.3:p.Pro969Thr
ENST00000637015.2:c.2995C>A	ENSP00000489729.2:p.Pro999Thr
ENST00000319584.11:c.1009C>A	ENSP00000313006.7:p.Pro337Thr
ENST00000346085.10:c.3034C>A	ENSP00000344546.5:p.Pro1012Thr
ENST00000350026.10:c.2746C>A	ENSP00000055163.7:p.Pro916Thr
ENST00000414678.7:c.1153C>A	ENSP00000412835.2:p.Pro385Thr
ENST00000452544.2:n.896C>A
ENST00000635849.1:c.316C>A	ENSP00000490948.1:p.Pro106Thr
ENST00000636426.1:n.129C>A
ENST00000636930.2:c.2995C>A MANE Select	ENSP00000490491.2:p.Pro999Thr
ENST00000637015.1:c.234C>A
ENST00000637568.1:c.38C>A
ENST00000637810.1:c.496C>A	ENSP00000489636.1:p.Pro166Thr
ENST00000637904.1:c.496C>A	ENSP00000490550.1:p.Pro166Thr
ENST00000647938.1:c.2785C>A	ENSP00000498155.1:p.Pro929Thr
ENST00000674190.1:n.1744C>A
ENST00000319584.10:c.1012C>A	ENSP00000313006.6:p.Pro338Thr
ENST00000346085.9:c.2785C>A	ENSP00000344546.4:p.Pro929Thr
ENST00000350026.9:c.2746C>A	ENSP00000055163.7:p.Pro916Thr
ENST00000414678.6:c.1153C>A	ENSP00000412835.2:p.Pro385Thr
ENST00000452544.1:n.842C>A
ENST00000478761.3:c.68C>A
NM_017519.2:c.2746C>A	NP_059989.2:p.Pro916Thr
NM_020732.3:c.2785C>A	NP_065783.3:p.Pro929Thr
XM_005267069.3:c.2746C>A	XP_005267126.2:p.Pro916Thr
XM_011535984.1:c.1696C>A	XP_011534286.1:p.Pro566Thr
XM_011535985.1:c.1516C>A	XP_011534287.1:p.Pro506Thr
XM_011535986.1:c.1276C>A	XP_011534288.1:p.Pro426Thr
XM_011535987.1:c.895C>A	XP_011534289.1:p.Pro299Thr
XM_011535988.1:c.-20+15650C>A	XP_011534290.1:n.-20+15650C>A
NM_001346813.1:c.2746C>A	NP_001333742.1:p.Pro916Thr
NM_001363725.1:c.496C>A	NP_001350654.1:p.Pro166Thr
XM_011535984.2:c.2827C>A	XP_011534286.2:p.Pro943Thr
XM_011535988.3:c.-20+15650C>A	XP_011534290.1:n.-20+15650C>A
XM_017011103.2:c.2827C>A	XP_016866592.1:p.Pro943Thr
XM_017011104.1:c.2827C>A	XP_016866593.1:p.Pro943Thr
XM_017011105.2:c.2827C>A	XP_016866594.1:p.Pro943Thr
XM_017011106.2:c.2827C>A	XP_016866595.1:p.Pro943Thr
XM_017011107.2:c.2647C>A	XP_016866596.1:p.Pro883Thr
XR_002956289.1:n.2910C>A
NM_001363725.2:c.496C>A	NP_001350654.1:p.Pro166Thr
NM_001371656.1:c.3034C>A	NP_001358585.1:p.Pro1012Thr
NM_001374820.1:c.3034C>A	NP_001361749.1:p.Pro1012Thr
NM_001374828.1:c.2995C>A MANE Select	NP_001361757.1:p.Pro999Thr
NM_017519.3:c.2995C>A	NP_059989.3:p.Pro999Thr