Canonical Allele Identifier: CA366388609

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469762C>A (hg19) ; chr6:g.157148628C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148628C>A , CM000668.2:g.157148628C>A	GRCh38
NC_000006.11:g.157469762C>A , CM000668.1:g.157469762C>A	GRCh37
NC_000006.10:g.157511454C>A	NCBI36
NG_032093.1:g.375699C>A
NG_032093.2:g.375699C>A
NG_066624.1:g.377603C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2766C>A	ENSP00000055163.8:p.Asn922Lys
ENST00000414678.8:c.2676C>A	ENSP00000412835.3:p.Asn892Lys
ENST00000637015.2:c.2766C>A	ENSP00000489729.2:p.Asn922Lys
ENST00000319584.11:c.780C>A	ENSP00000313006.7:p.Asn260Lys
ENST00000346085.10:c.2805C>A	ENSP00000344546.5:p.Asn935Lys
ENST00000350026.10:c.2517C>A	ENSP00000055163.7:p.Asn839Lys
ENST00000414678.7:c.924C>A	ENSP00000412835.2:p.Asn308Lys
ENST00000452544.2:n.667C>A
ENST00000635849.1:c.87C>A	ENSP00000490948.1:p.Asn29Lys
ENST00000636930.2:c.2766C>A MANE Select	ENSP00000490491.2:p.Asn922Lys
ENST00000637015.1:c.5C>A
ENST00000637810.1:c.267C>A	ENSP00000489636.1:p.Asn89Lys
ENST00000637904.1:c.267C>A	ENSP00000490550.1:p.Asn89Lys
ENST00000647938.1:c.2556C>A	ENSP00000498155.1:p.Asn852Lys
ENST00000674190.1:n.1515C>A
ENST00000319584.10:c.783C>A	ENSP00000313006.6:p.Asn261Lys
ENST00000346085.9:c.2556C>A	ENSP00000344546.4:p.Asn852Lys
ENST00000350026.9:c.2517C>A	ENSP00000055163.7:p.Asn839Lys
ENST00000414678.6:c.924C>A	ENSP00000412835.2:p.Asn308Lys
ENST00000452544.1:n.613C>A
NM_017519.2:c.2517C>A	NP_059989.2:p.Asn839Lys
NM_020732.3:c.2556C>A	NP_065783.3:p.Asn852Lys
XM_005267069.3:c.2517C>A	XP_005267126.2:p.Asn839Lys
XM_011535984.1:c.1467C>A	XP_011534286.1:p.Asn489Lys
XM_011535985.1:c.1287C>A	XP_011534287.1:p.Asn429Lys
XM_011535986.1:c.1047C>A	XP_011534288.1:p.Asn349Lys
XM_011535987.1:c.666C>A	XP_011534289.1:p.Asn222Lys
XM_011535988.1:c.-20+15421C>A	XP_011534290.1:n.-20+15421C>A
NM_001346813.1:c.2517C>A	NP_001333742.1:p.Asn839Lys
NM_001363725.1:c.267C>A	NP_001350654.1:p.Asn89Lys
XM_011535984.2:c.2598C>A	XP_011534286.2:p.Asn866Lys
XM_011535988.3:c.-20+15421C>A	XP_011534290.1:n.-20+15421C>A
XM_017011103.2:c.2598C>A	XP_016866592.1:p.Asn866Lys
XM_017011104.1:c.2598C>A	XP_016866593.1:p.Asn866Lys
XM_017011105.2:c.2598C>A	XP_016866594.1:p.Asn866Lys
XM_017011106.2:c.2598C>A	XP_016866595.1:p.Asn866Lys
XM_017011107.2:c.2418C>A	XP_016866596.1:p.Asn806Lys
XR_002956289.1:n.2681C>A
NM_001363725.2:c.267C>A	NP_001350654.1:p.Asn89Lys
NM_001371656.1:c.2805C>A	NP_001358585.1:p.Asn935Lys
NM_001374820.1:c.2805C>A	NP_001361749.1:p.Asn935Lys
NM_001374828.1:c.2766C>A MANE Select	NP_001361757.1:p.Asn922Lys
NM_017519.3:c.2766C>A	NP_059989.3:p.Asn922Lys