Canonical Allele Identifier: CA366389125

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469999G>A (hg19) ; chr6:g.157148865G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148865G>A , CM000668.2:g.157148865G>A	GRCh38
NC_000006.11:g.157469999G>A , CM000668.1:g.157469999G>A	GRCh37
NC_000006.10:g.157511691G>A	NCBI36
NG_032093.1:g.375936G>A
NG_032093.2:g.375936G>A
NG_066624.1:g.377840G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3003G>A	ENSP00000055163.8:p.Met1001Ile
ENST00000414678.8:c.2913G>A	ENSP00000412835.3:p.Met971Ile
ENST00000637015.2:c.3003G>A	ENSP00000489729.2:p.Met1001Ile
ENST00000319584.11:c.1017G>A	ENSP00000313006.7:p.Met339Ile
ENST00000346085.10:c.3042G>A	ENSP00000344546.5:p.Met1014Ile
ENST00000350026.10:c.2754G>A	ENSP00000055163.7:p.Met918Ile
ENST00000414678.7:c.1161G>A	ENSP00000412835.2:p.Met387Ile
ENST00000452544.2:n.904G>A
ENST00000635849.1:c.324G>A	ENSP00000490948.1:p.Met108Ile
ENST00000636426.1:n.137G>A
ENST00000636930.2:c.3003G>A MANE Select	ENSP00000490491.2:p.Met1001Ile
ENST00000637015.1:c.242G>A
ENST00000637568.1:c.46G>A
ENST00000637810.1:c.504G>A	ENSP00000489636.1:p.Met168Ile
ENST00000637904.1:c.504G>A	ENSP00000490550.1:p.Met168Ile
ENST00000647938.1:c.2793G>A	ENSP00000498155.1:p.Met931Ile
ENST00000674190.1:n.1752G>A
ENST00000319584.10:c.1020G>A	ENSP00000313006.6:p.Met340Ile
ENST00000346085.9:c.2793G>A	ENSP00000344546.4:p.Met931Ile
ENST00000350026.9:c.2754G>A	ENSP00000055163.7:p.Met918Ile
ENST00000414678.6:c.1161G>A	ENSP00000412835.2:p.Met387Ile
ENST00000452544.1:n.850G>A
ENST00000478761.3:c.76G>A
NM_017519.2:c.2754G>A	NP_059989.2:p.Met918Ile
NM_020732.3:c.2793G>A	NP_065783.3:p.Met931Ile
XM_005267069.3:c.2754G>A	XP_005267126.2:p.Met918Ile
XM_011535984.1:c.1704G>A	XP_011534286.1:p.Met568Ile
XM_011535985.1:c.1524G>A	XP_011534287.1:p.Met508Ile
XM_011535986.1:c.1284G>A	XP_011534288.1:p.Met428Ile
XM_011535987.1:c.903G>A	XP_011534289.1:p.Met301Ile
XM_011535988.1:c.-20+15658G>A	XP_011534290.1:n.-20+15658G>A
NM_001346813.1:c.2754G>A	NP_001333742.1:p.Met918Ile
NM_001363725.1:c.504G>A	NP_001350654.1:p.Met168Ile
XM_011535984.2:c.2835G>A	XP_011534286.2:p.Met945Ile
XM_011535988.3:c.-20+15658G>A	XP_011534290.1:n.-20+15658G>A
XM_017011103.2:c.2835G>A	XP_016866592.1:p.Met945Ile
XM_017011104.1:c.2835G>A	XP_016866593.1:p.Met945Ile
XM_017011105.2:c.2835G>A	XP_016866594.1:p.Met945Ile
XM_017011106.2:c.2835G>A	XP_016866595.1:p.Met945Ile
XM_017011107.2:c.2655G>A	XP_016866596.1:p.Met885Ile
XR_002956289.1:n.2918G>A
NM_001363725.2:c.504G>A	NP_001350654.1:p.Met168Ile
NM_001371656.1:c.3042G>A	NP_001358585.1:p.Met1014Ile
NM_001374820.1:c.3042G>A	NP_001361749.1:p.Met1014Ile
NM_001374828.1:c.3003G>A MANE Select	NP_001361757.1:p.Met1001Ile
NM_017519.3:c.3003G>A	NP_059989.3:p.Met1001Ile