Canonical Allele Identifier: CA366228291

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502275T>C (hg19) ; chr6:g.157181141T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181141T>C , CM000668.2:g.157181141T>C	GRCh38
NC_000006.11:g.157502275T>C , CM000668.1:g.157502275T>C	GRCh37
NC_000006.10:g.157543967T>C	NCBI36
NG_032093.1:g.408212T>C
NG_032093.2:g.408212T>C
NG_066624.1:g.410116T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3518T>C	ENSP00000055163.8:p.Leu1173Pro
ENST00000414678.8:c.3587T>C	ENSP00000412835.3:p.Leu1196Pro
ENST00000637015.2:c.3806T>C	ENSP00000489729.2:p.Leu1269Pro
ENST00000319584.11:c.1691T>C	ENSP00000313006.7:p.Leu564Pro
ENST00000346085.10:c.3557T>C	ENSP00000344546.5:p.Leu1186Pro
ENST00000350026.10:c.3269T>C	ENSP00000055163.7:p.Leu1090Pro
ENST00000414678.7:c.1835T>C	ENSP00000412835.2:p.Leu612Pro
ENST00000635849.1:c.998T>C	ENSP00000490948.1:p.Leu333Pro
ENST00000635957.1:c.632T>C	ENSP00000490385.1:p.Leu211Pro
ENST00000636930.2:c.3677T>C MANE Select	ENSP00000490491.2:p.Leu1226Pro
ENST00000636940.1:n.1674T>C
ENST00000637015.1:c.1045T>C
ENST00000637568.1:c.959T>C
ENST00000637741.1:n.343T>C
ENST00000637810.1:c.1019T>C	ENSP00000489636.1:p.Leu340Pro
ENST00000637904.1:c.1178T>C	ENSP00000490550.1:p.Leu393Pro
ENST00000647938.1:c.3308T>C	ENSP00000498155.1:p.Leu1103Pro
ENST00000319584.10:c.1694T>C	ENSP00000313006.6:p.Leu565Pro
ENST00000346085.9:c.3308T>C	ENSP00000344546.4:p.Leu1103Pro
ENST00000350026.9:c.3269T>C	ENSP00000055163.7:p.Leu1090Pro
ENST00000400790.3:c.470T>C	ENSP00000383596.3:p.Leu157Pro
ENST00000414678.6:c.1835T>C	ENSP00000412835.2:p.Leu612Pro
ENST00000478761.3:c.879T>C
NM_017519.2:c.3269T>C	NP_059989.2:p.Leu1090Pro
NM_020732.3:c.3308T>C	NP_065783.3:p.Leu1103Pro
XM_005267069.3:c.3428T>C	XP_005267126.2:p.Leu1143Pro
XM_011535984.1:c.2507T>C	XP_011534286.1:p.Leu836Pro
XM_011535985.1:c.2327T>C	XP_011534287.1:p.Leu776Pro
XM_011535986.1:c.2087T>C	XP_011534288.1:p.Leu696Pro
XM_011535987.1:c.1706T>C	XP_011534289.1:p.Leu569Pro
XM_011535988.1:c.569T>C	XP_011534290.1:p.Leu190Pro
NM_001346813.1:c.3428T>C	NP_001333742.1:p.Leu1143Pro
NM_001363725.1:c.1178T>C	NP_001350654.1:p.Leu393Pro
XM_011535984.2:c.3638T>C	XP_011534286.2:p.Leu1213Pro
XM_011535988.3:c.569T>C	XP_011534290.1:p.Leu190Pro
XM_017011103.2:c.3539T>C	XP_016866592.1:p.Leu1180Pro
XM_017011104.1:c.3509T>C	XP_016866593.1:p.Leu1170Pro
XM_017011105.2:c.3479T>C	XP_016866594.1:p.Leu1160Pro
XM_017011106.2:c.3350T>C	XP_016866595.1:p.Leu1117Pro
XM_017011107.2:c.3329T>C	XP_016866596.1:p.Leu1110Pro
XR_002956289.1:n.3721T>C
NM_001363725.2:c.1178T>C	NP_001350654.1:p.Leu393Pro
NM_001371656.1:c.3557T>C	NP_001358585.1:p.Leu1186Pro
NM_001374820.1:c.3557T>C	NP_001361749.1:p.Leu1186Pro
NM_001374828.1:c.3677T>C MANE Select	NP_001361757.1:p.Leu1226Pro
NM_017519.3:c.3518T>C	NP_059989.3:p.Leu1173Pro