Canonical Allele Identifier: CA366241885

Gene: ARID1B

Linked Data

• dbSNP Id: rs1794073907
• MyVariant Identifiers: chr6:g.157522217G>C (hg19) ; chr6:g.157201083G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201083G>C , CM000668.2:g.157201083G>C	GRCh38
NC_000006.11:g.157522217G>C , CM000668.1:g.157522217G>C	GRCh37
NC_000006.10:g.157563909G>C	NCBI36
NG_032093.1:g.428154G>C
NG_032093.2:g.428154G>C
NG_066624.1:g.430058G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4699G>C	ENSP00000055163.8:p.Asp1567His
ENST00000414678.8:c.4768G>C	ENSP00000412835.3:p.Asp1590His
ENST00000637015.2:c.4987G>C	ENSP00000489729.2:p.Asp1663His
ENST00000346085.10:c.4738G>C	ENSP00000344546.5:p.Asp1580His
ENST00000350026.10:c.4450G>C	ENSP00000055163.7:p.Asp1484His
ENST00000414678.7:c.3016G>C	ENSP00000412835.2:p.Asp1006His
ENST00000635849.1:c.2179G>C	ENSP00000490948.1:p.Asp727His
ENST00000635957.1:c.1810G>C	ENSP00000490385.1:p.Asp604His
ENST00000636227.1:n.3321G>C
ENST00000636254.1:n.778G>C
ENST00000636930.2:c.4858G>C MANE Select	ENSP00000490491.2:p.Asp1620His
ENST00000636940.1:n.2855G>C
ENST00000637015.1:c.2226G>C
ENST00000637568.1:c.2140G>C
ENST00000637741.1:n.1524G>C
ENST00000637810.1:c.2200G>C	ENSP00000489636.1:p.Asp734His
ENST00000637904.1:c.2359G>C	ENSP00000490550.1:p.Asp787His
ENST00000647938.1:c.4489G>C	ENSP00000498155.1:p.Asp1497His
ENST00000346085.9:c.4489G>C	ENSP00000344546.4:p.Asp1497His
ENST00000350026.9:c.4450G>C	ENSP00000055163.7:p.Asp1484His
ENST00000414678.6:c.3016G>C	ENSP00000412835.2:p.Asp1006His
NM_017519.2:c.4450G>C	NP_059989.2:p.Asp1484His
NM_020732.3:c.4489G>C	NP_065783.3:p.Asp1497His
XM_005267069.3:c.4609G>C	XP_005267126.2:p.Asp1537His
XM_011535984.1:c.3688G>C	XP_011534286.1:p.Asp1230His
XM_011535985.1:c.3508G>C	XP_011534287.1:p.Asp1170His
XM_011535986.1:c.3268G>C	XP_011534288.1:p.Asp1090His
XM_011535987.1:c.2887G>C	XP_011534289.1:p.Asp963His
XM_011535988.1:c.1750G>C	XP_011534290.1:p.Asp584His
NM_001346813.1:c.4609G>C	NP_001333742.1:p.Asp1537His
NM_001363725.1:c.2359G>C	NP_001350654.1:p.Asp787His
XM_011535984.2:c.4819G>C	XP_011534286.2:p.Asp1607His
XM_011535988.3:c.1750G>C	XP_011534290.1:p.Asp584His
XM_017011103.2:c.4720G>C	XP_016866592.1:p.Asp1574His
XM_017011104.1:c.4690G>C	XP_016866593.1:p.Asp1564His
XM_017011105.2:c.4660G>C	XP_016866594.1:p.Asp1554His
XM_017011106.2:c.4531G>C	XP_016866595.1:p.Asp1511His
XM_017011107.2:c.4510G>C	XP_016866596.1:p.Asp1504His
XR_002956289.1:n.4805G>C
NM_001363725.2:c.2359G>C	NP_001350654.1:p.Asp787His
NM_001371656.1:c.4738G>C	NP_001358585.1:p.Asp1580His
NM_001374820.1:c.4738G>C	NP_001361749.1:p.Asp1580His
NM_001374828.1:c.4858G>C MANE Select	NP_001361757.1:p.Asp1620His
NM_017519.3:c.4699G>C	NP_059989.3:p.Asp1567His