Canonical Allele Identifier: CA366228076

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317403
• MyVariant Identifiers: chr6:g.157502238C>A (hg19) ; chr6:g.157181104C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181104C>A , CM000668.2:g.157181104C>A	GRCh38
NC_000006.11:g.157502238C>A , CM000668.1:g.157502238C>A	GRCh37
NC_000006.10:g.157543930C>A	NCBI36
NG_032093.1:g.408175C>A
NG_032093.2:g.408175C>A
NG_066624.1:g.410079C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3481C>A	ENSP00000055163.8:p.Pro1161Thr
ENST00000414678.8:c.3550C>A	ENSP00000412835.3:p.Pro1184Thr
ENST00000637015.2:c.3769C>A	ENSP00000489729.2:p.Pro1257Thr
ENST00000319584.11:c.1654C>A	ENSP00000313006.7:p.Pro552Thr
ENST00000346085.10:c.3520C>A	ENSP00000344546.5:p.Pro1174Thr
ENST00000350026.10:c.3232C>A	ENSP00000055163.7:p.Pro1078Thr
ENST00000414678.7:c.1798C>A	ENSP00000412835.2:p.Pro600Thr
ENST00000635849.1:c.961C>A	ENSP00000490948.1:p.Pro321Thr
ENST00000635957.1:c.595C>A	ENSP00000490385.1:p.Pro199Thr
ENST00000636930.2:c.3640C>A MANE Select	ENSP00000490491.2:p.Pro1214Thr
ENST00000636940.1:n.1637C>A
ENST00000637015.1:c.1008C>A
ENST00000637568.1:c.922C>A
ENST00000637741.1:n.306C>A
ENST00000637810.1:c.982C>A	ENSP00000489636.1:p.Pro328Thr
ENST00000637904.1:c.1141C>A	ENSP00000490550.1:p.Pro381Thr
ENST00000647938.1:c.3271C>A	ENSP00000498155.1:p.Pro1091Thr
ENST00000319584.10:c.1657C>A	ENSP00000313006.6:p.Pro553Thr
ENST00000346085.9:c.3271C>A	ENSP00000344546.4:p.Pro1091Thr
ENST00000350026.9:c.3232C>A	ENSP00000055163.7:p.Pro1078Thr
ENST00000400790.3:c.433C>A	ENSP00000383596.3:p.Pro145Thr
ENST00000414678.6:c.1798C>A	ENSP00000412835.2:p.Pro600Thr
ENST00000478761.3:c.842C>A
NM_017519.2:c.3232C>A	NP_059989.2:p.Pro1078Thr
NM_020732.3:c.3271C>A	NP_065783.3:p.Pro1091Thr
XM_005267069.3:c.3391C>A	XP_005267126.2:p.Pro1131Thr
XM_011535984.1:c.2470C>A	XP_011534286.1:p.Pro824Thr
XM_011535985.1:c.2290C>A	XP_011534287.1:p.Pro764Thr
XM_011535986.1:c.2050C>A	XP_011534288.1:p.Pro684Thr
XM_011535987.1:c.1669C>A	XP_011534289.1:p.Pro557Thr
XM_011535988.1:c.532C>A	XP_011534290.1:p.Pro178Thr
NM_001346813.1:c.3391C>A	NP_001333742.1:p.Pro1131Thr
NM_001363725.1:c.1141C>A	NP_001350654.1:p.Pro381Thr
XM_011535984.2:c.3601C>A	XP_011534286.2:p.Pro1201Thr
XM_011535988.3:c.532C>A	XP_011534290.1:p.Pro178Thr
XM_017011103.2:c.3502C>A	XP_016866592.1:p.Pro1168Thr
XM_017011104.1:c.3472C>A	XP_016866593.1:p.Pro1158Thr
XM_017011105.2:c.3442C>A	XP_016866594.1:p.Pro1148Thr
XM_017011106.2:c.3313C>A	XP_016866595.1:p.Pro1105Thr
XM_017011107.2:c.3292C>A	XP_016866596.1:p.Pro1098Thr
XR_002956289.1:n.3684C>A
NM_001363725.2:c.1141C>A	NP_001350654.1:p.Pro381Thr
NM_001371656.1:c.3520C>A	NP_001358585.1:p.Pro1174Thr
NM_001374820.1:c.3520C>A	NP_001361749.1:p.Pro1174Thr
NM_001374828.1:c.3640C>A MANE Select	NP_001361757.1:p.Pro1214Thr
NM_017519.3:c.3481C>A	NP_059989.3:p.Pro1161Thr