Canonical Allele Identifier: CA366388619

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469766T>A (hg19) ; chr6:g.157148632T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148632T>A , CM000668.2:g.157148632T>A	GRCh38
NC_000006.11:g.157469766T>A , CM000668.1:g.157469766T>A	GRCh37
NC_000006.10:g.157511458T>A	NCBI36
NG_032093.1:g.375703T>A
NG_032093.2:g.375703T>A
NG_066624.1:g.377607T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2770T>A	ENSP00000055163.8:p.Ser924Thr
ENST00000414678.8:c.2680T>A	ENSP00000412835.3:p.Ser894Thr
ENST00000637015.2:c.2770T>A	ENSP00000489729.2:p.Ser924Thr
ENST00000319584.11:c.784T>A	ENSP00000313006.7:p.Ser262Thr
ENST00000346085.10:c.2809T>A	ENSP00000344546.5:p.Ser937Thr
ENST00000350026.10:c.2521T>A	ENSP00000055163.7:p.Ser841Thr
ENST00000414678.7:c.928T>A	ENSP00000412835.2:p.Ser310Thr
ENST00000452544.2:n.671T>A
ENST00000635849.1:c.91T>A	ENSP00000490948.1:p.Ser31Thr
ENST00000636930.2:c.2770T>A MANE Select	ENSP00000490491.2:p.Ser924Thr
ENST00000637015.1:c.9T>A
ENST00000637810.1:c.271T>A	ENSP00000489636.1:p.Ser91Thr
ENST00000637904.1:c.271T>A	ENSP00000490550.1:p.Ser91Thr
ENST00000647938.1:c.2560T>A	ENSP00000498155.1:p.Ser854Thr
ENST00000674190.1:n.1519T>A
ENST00000319584.10:c.787T>A	ENSP00000313006.6:p.Ser263Thr
ENST00000346085.9:c.2560T>A	ENSP00000344546.4:p.Ser854Thr
ENST00000350026.9:c.2521T>A	ENSP00000055163.7:p.Ser841Thr
ENST00000414678.6:c.928T>A	ENSP00000412835.2:p.Ser310Thr
ENST00000452544.1:n.617T>A
NM_017519.2:c.2521T>A	NP_059989.2:p.Ser841Thr
NM_020732.3:c.2560T>A	NP_065783.3:p.Ser854Thr
XM_005267069.3:c.2521T>A	XP_005267126.2:p.Ser841Thr
XM_011535984.1:c.1471T>A	XP_011534286.1:p.Ser491Thr
XM_011535985.1:c.1291T>A	XP_011534287.1:p.Ser431Thr
XM_011535986.1:c.1051T>A	XP_011534288.1:p.Ser351Thr
XM_011535987.1:c.670T>A	XP_011534289.1:p.Ser224Thr
XM_011535988.1:c.-20+15425T>A	XP_011534290.1:n.-20+15425T>A
NM_001346813.1:c.2521T>A	NP_001333742.1:p.Ser841Thr
NM_001363725.1:c.271T>A	NP_001350654.1:p.Ser91Thr
XM_011535984.2:c.2602T>A	XP_011534286.2:p.Ser868Thr
XM_011535988.3:c.-20+15425T>A	XP_011534290.1:n.-20+15425T>A
XM_017011103.2:c.2602T>A	XP_016866592.1:p.Ser868Thr
XM_017011104.1:c.2602T>A	XP_016866593.1:p.Ser868Thr
XM_017011105.2:c.2602T>A	XP_016866594.1:p.Ser868Thr
XM_017011106.2:c.2602T>A	XP_016866595.1:p.Ser868Thr
XM_017011107.2:c.2422T>A	XP_016866596.1:p.Ser808Thr
XR_002956289.1:n.2685T>A
NM_001363725.2:c.271T>A	NP_001350654.1:p.Ser91Thr
NM_001371656.1:c.2809T>A	NP_001358585.1:p.Ser937Thr
NM_001374820.1:c.2809T>A	NP_001361749.1:p.Ser937Thr
NM_001374828.1:c.2770T>A MANE Select	NP_001361757.1:p.Ser924Thr
NM_017519.3:c.2770T>A	NP_059989.3:p.Ser924Thr