Canonical Allele Identifier: CA366241557

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522157A>C (hg19) ; chr6:g.157201023A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201023A>C , CM000668.2:g.157201023A>C	GRCh38
NC_000006.11:g.157522157A>C , CM000668.1:g.157522157A>C	GRCh37
NC_000006.10:g.157563849A>C	NCBI36
NG_032093.1:g.428094A>C
NG_032093.2:g.428094A>C
NG_066624.1:g.429998A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4639A>C	ENSP00000055163.8:p.Asn1547His
ENST00000414678.8:c.4708A>C	ENSP00000412835.3:p.Asn1570His
ENST00000637015.2:c.4927A>C	ENSP00000489729.2:p.Asn1643His
ENST00000346085.10:c.4678A>C	ENSP00000344546.5:p.Asn1560His
ENST00000350026.10:c.4390A>C	ENSP00000055163.7:p.Asn1464His
ENST00000414678.7:c.2956A>C	ENSP00000412835.2:p.Asn986His
ENST00000635849.1:c.2119A>C	ENSP00000490948.1:p.Asn707His
ENST00000635957.1:c.1750A>C	ENSP00000490385.1:p.Asn584His
ENST00000636227.1:n.3261A>C
ENST00000636254.1:n.718A>C
ENST00000636930.2:c.4798A>C MANE Select	ENSP00000490491.2:p.Asn1600His
ENST00000636940.1:n.2795A>C
ENST00000637015.1:c.2166A>C
ENST00000637568.1:c.2080A>C
ENST00000637741.1:n.1464A>C
ENST00000637810.1:c.2140A>C	ENSP00000489636.1:p.Asn714His
ENST00000637904.1:c.2299A>C	ENSP00000490550.1:p.Asn767His
ENST00000647938.1:c.4429A>C	ENSP00000498155.1:p.Asn1477His
ENST00000346085.9:c.4429A>C	ENSP00000344546.4:p.Asn1477His
ENST00000350026.9:c.4390A>C	ENSP00000055163.7:p.Asn1464His
ENST00000414678.6:c.2956A>C	ENSP00000412835.2:p.Asn986His
NM_017519.2:c.4390A>C	NP_059989.2:p.Asn1464His
NM_020732.3:c.4429A>C	NP_065783.3:p.Asn1477His
XM_005267069.3:c.4549A>C	XP_005267126.2:p.Asn1517His
XM_011535984.1:c.3628A>C	XP_011534286.1:p.Asn1210His
XM_011535985.1:c.3448A>C	XP_011534287.1:p.Asn1150His
XM_011535986.1:c.3208A>C	XP_011534288.1:p.Asn1070His
XM_011535987.1:c.2827A>C	XP_011534289.1:p.Asn943His
XM_011535988.1:c.1690A>C	XP_011534290.1:p.Asn564His
NM_001346813.1:c.4549A>C	NP_001333742.1:p.Asn1517His
NM_001363725.1:c.2299A>C	NP_001350654.1:p.Asn767His
XM_011535984.2:c.4759A>C	XP_011534286.2:p.Asn1587His
XM_011535988.3:c.1690A>C	XP_011534290.1:p.Asn564His
XM_017011103.2:c.4660A>C	XP_016866592.1:p.Asn1554His
XM_017011104.1:c.4630A>C	XP_016866593.1:p.Asn1544His
XM_017011105.2:c.4600A>C	XP_016866594.1:p.Asn1534His
XM_017011106.2:c.4471A>C	XP_016866595.1:p.Asn1491His
XM_017011107.2:c.4450A>C	XP_016866596.1:p.Asn1484His
XR_002956289.1:n.4745A>C
NM_001363725.2:c.2299A>C	NP_001350654.1:p.Asn767His
NM_001371656.1:c.4678A>C	NP_001358585.1:p.Asn1560His
NM_001374820.1:c.4678A>C	NP_001361749.1:p.Asn1560His
NM_001374828.1:c.4798A>C MANE Select	NP_001361757.1:p.Asn1600His
NM_017519.3:c.4639A>C	NP_059989.3:p.Asn1547His