Canonical Allele Identifier: CA366228470

Gene: ARID1B

Linked Data

• dbSNP Id: rs375581771
• MyVariant Identifiers: chr6:g.157502296T>C (hg19) ; chr6:g.157181162T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181162T>C , CM000668.2:g.157181162T>C	GRCh38
NC_000006.11:g.157502296T>C , CM000668.1:g.157502296T>C	GRCh37
NC_000006.10:g.157543988T>C	NCBI36
NG_032093.1:g.408233T>C
NG_032093.2:g.408233T>C
NG_066624.1:g.410137T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3539T>C	ENSP00000055163.8:p.Ile1180Thr
ENST00000414678.8:c.3608T>C	ENSP00000412835.3:p.Ile1203Thr
ENST00000637015.2:c.3827T>C	ENSP00000489729.2:p.Ile1276Thr
ENST00000319584.11:c.1712T>C	ENSP00000313006.7:p.Ile571Thr
ENST00000346085.10:c.3578T>C	ENSP00000344546.5:p.Ile1193Thr
ENST00000350026.10:c.3290T>C	ENSP00000055163.7:p.Ile1097Thr
ENST00000414678.7:c.1856T>C	ENSP00000412835.2:p.Ile619Thr
ENST00000635849.1:c.1019T>C	ENSP00000490948.1:p.Ile340Thr
ENST00000635957.1:c.653T>C	ENSP00000490385.1:p.Ile218Thr
ENST00000636930.2:c.3698T>C MANE Select	ENSP00000490491.2:p.Ile1233Thr
ENST00000636940.1:n.1695T>C
ENST00000637015.1:c.1066T>C
ENST00000637568.1:c.980T>C
ENST00000637741.1:n.364T>C
ENST00000637810.1:c.1040T>C	ENSP00000489636.1:p.Ile347Thr
ENST00000637904.1:c.1199T>C	ENSP00000490550.1:p.Ile400Thr
ENST00000647938.1:c.3329T>C	ENSP00000498155.1:p.Ile1110Thr
ENST00000319584.10:c.1715T>C	ENSP00000313006.6:p.Ile572Thr
ENST00000346085.9:c.3329T>C	ENSP00000344546.4:p.Ile1110Thr
ENST00000350026.9:c.3290T>C	ENSP00000055163.7:p.Ile1097Thr
ENST00000400790.3:c.491T>C	ENSP00000383596.3:p.Ile164Thr
ENST00000414678.6:c.1856T>C	ENSP00000412835.2:p.Ile619Thr
ENST00000478761.3:c.900T>C
NM_017519.2:c.3290T>C	NP_059989.2:p.Ile1097Thr
NM_020732.3:c.3329T>C	NP_065783.3:p.Ile1110Thr
XM_005267069.3:c.3449T>C	XP_005267126.2:p.Ile1150Thr
XM_011535984.1:c.2528T>C	XP_011534286.1:p.Ile843Thr
XM_011535985.1:c.2348T>C	XP_011534287.1:p.Ile783Thr
XM_011535986.1:c.2108T>C	XP_011534288.1:p.Ile703Thr
XM_011535987.1:c.1727T>C	XP_011534289.1:p.Ile576Thr
XM_011535988.1:c.590T>C	XP_011534290.1:p.Ile197Thr
NM_001346813.1:c.3449T>C	NP_001333742.1:p.Ile1150Thr
NM_001363725.1:c.1199T>C	NP_001350654.1:p.Ile400Thr
XM_011535984.2:c.3659T>C	XP_011534286.2:p.Ile1220Thr
XM_011535988.3:c.590T>C	XP_011534290.1:p.Ile197Thr
XM_017011103.2:c.3560T>C	XP_016866592.1:p.Ile1187Thr
XM_017011104.1:c.3530T>C	XP_016866593.1:p.Ile1177Thr
XM_017011105.2:c.3500T>C	XP_016866594.1:p.Ile1167Thr
XM_017011106.2:c.3371T>C	XP_016866595.1:p.Ile1124Thr
XM_017011107.2:c.3350T>C	XP_016866596.1:p.Ile1117Thr
XR_002956289.1:n.3742T>C
NM_001363725.2:c.1199T>C	NP_001350654.1:p.Ile400Thr
NM_001371656.1:c.3578T>C	NP_001358585.1:p.Ile1193Thr
NM_001374820.1:c.3578T>C	NP_001361749.1:p.Ile1193Thr
NM_001374828.1:c.3698T>C MANE Select	NP_001361757.1:p.Ile1233Thr
NM_017519.3:c.3539T>C	NP_059989.3:p.Ile1180Thr