Canonical Allele Identifier: CA366227638

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317127
• MyVariant Identifiers: chr6:g.157502193T>C (hg19) ; chr6:g.157181059T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181059T>C , CM000668.2:g.157181059T>C	GRCh38
NC_000006.11:g.157502193T>C , CM000668.1:g.157502193T>C	GRCh37
NC_000006.10:g.157543885T>C	NCBI36
NG_032093.1:g.408130T>C
NG_032093.2:g.408130T>C
NG_066624.1:g.410034T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3436T>C	ENSP00000055163.8:p.Tyr1146His
ENST00000414678.8:c.3505T>C	ENSP00000412835.3:p.Tyr1169His
ENST00000637015.2:c.3724T>C	ENSP00000489729.2:p.Tyr1242His
ENST00000319584.11:c.1609T>C	ENSP00000313006.7:p.Tyr537His
ENST00000346085.10:c.3475T>C	ENSP00000344546.5:p.Tyr1159His
ENST00000350026.10:c.3187T>C	ENSP00000055163.7:p.Tyr1063His
ENST00000414678.7:c.1753T>C	ENSP00000412835.2:p.Tyr585His
ENST00000635849.1:c.916T>C	ENSP00000490948.1:p.Tyr306His
ENST00000635957.1:c.550T>C	ENSP00000490385.1:p.Tyr184His
ENST00000636930.2:c.3595T>C MANE Select	ENSP00000490491.2:p.Tyr1199His
ENST00000636940.1:n.1592T>C
ENST00000637015.1:c.963T>C
ENST00000637568.1:c.877T>C
ENST00000637741.1:n.261T>C
ENST00000637810.1:c.937T>C	ENSP00000489636.1:p.Tyr313His
ENST00000637904.1:c.1096T>C	ENSP00000490550.1:p.Tyr366His
ENST00000647938.1:c.3226T>C	ENSP00000498155.1:p.Tyr1076His
ENST00000319584.10:c.1612T>C	ENSP00000313006.6:p.Tyr538His
ENST00000346085.9:c.3226T>C	ENSP00000344546.4:p.Tyr1076His
ENST00000350026.9:c.3187T>C	ENSP00000055163.7:p.Tyr1063His
ENST00000400790.3:c.388T>C	ENSP00000383596.3:p.Tyr130His
ENST00000414678.6:c.1753T>C	ENSP00000412835.2:p.Tyr585His
ENST00000478761.3:c.797T>C
NM_017519.2:c.3187T>C	NP_059989.2:p.Tyr1063His
NM_020732.3:c.3226T>C	NP_065783.3:p.Tyr1076His
XM_005267069.3:c.3346T>C	XP_005267126.2:p.Tyr1116His
XM_011535984.1:c.2425T>C	XP_011534286.1:p.Tyr809His
XM_011535985.1:c.2245T>C	XP_011534287.1:p.Tyr749His
XM_011535986.1:c.2005T>C	XP_011534288.1:p.Tyr669His
XM_011535987.1:c.1624T>C	XP_011534289.1:p.Tyr542His
XM_011535988.1:c.487T>C	XP_011534290.1:p.Tyr163His
NM_001346813.1:c.3346T>C	NP_001333742.1:p.Tyr1116His
NM_001363725.1:c.1096T>C	NP_001350654.1:p.Tyr366His
XM_011535984.2:c.3556T>C	XP_011534286.2:p.Tyr1186His
XM_011535988.3:c.487T>C	XP_011534290.1:p.Tyr163His
XM_017011103.2:c.3457T>C	XP_016866592.1:p.Tyr1153His
XM_017011104.1:c.3427T>C	XP_016866593.1:p.Tyr1143His
XM_017011105.2:c.3397T>C	XP_016866594.1:p.Tyr1133His
XM_017011106.2:c.3268T>C	XP_016866595.1:p.Tyr1090His
XM_017011107.2:c.3247T>C	XP_016866596.1:p.Tyr1083His
XR_002956289.1:n.3639T>C
NM_001363725.2:c.1096T>C	NP_001350654.1:p.Tyr366His
NM_001371656.1:c.3475T>C	NP_001358585.1:p.Tyr1159His
NM_001374820.1:c.3475T>C	NP_001361749.1:p.Tyr1159His
NM_001374828.1:c.3595T>C MANE Select	NP_001361757.1:p.Tyr1199His
NM_017519.3:c.3436T>C	NP_059989.3:p.Tyr1146His