Canonical Allele Identifier: CA366389013

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469948C>A (hg19) ; chr6:g.157148814C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148814C>A , CM000668.2:g.157148814C>A	GRCh38
NC_000006.11:g.157469948C>A , CM000668.1:g.157469948C>A	GRCh37
NC_000006.10:g.157511640C>A	NCBI36
NG_032093.1:g.375885C>A
NG_032093.2:g.375885C>A
NG_066624.1:g.377789C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2952C>A	ENSP00000055163.8:p.Ser984Arg
ENST00000414678.8:c.2862C>A	ENSP00000412835.3:p.Ser954Arg
ENST00000637015.2:c.2952C>A	ENSP00000489729.2:p.Ser984Arg
ENST00000319584.11:c.966C>A	ENSP00000313006.7:p.Ser322Arg
ENST00000346085.10:c.2991C>A	ENSP00000344546.5:p.Ser997Arg
ENST00000350026.10:c.2703C>A	ENSP00000055163.7:p.Ser901Arg
ENST00000414678.7:c.1110C>A	ENSP00000412835.2:p.Ser370Arg
ENST00000452544.2:n.853C>A
ENST00000635849.1:c.273C>A	ENSP00000490948.1:p.Ser91Arg
ENST00000636426.1:n.86C>A
ENST00000636930.2:c.2952C>A MANE Select	ENSP00000490491.2:p.Ser984Arg
ENST00000637015.1:c.191C>A
ENST00000637810.1:c.453C>A	ENSP00000489636.1:p.Ser151Arg
ENST00000637904.1:c.453C>A	ENSP00000490550.1:p.Ser151Arg
ENST00000647938.1:c.2742C>A	ENSP00000498155.1:p.Ser914Arg
ENST00000674190.1:n.1701C>A
ENST00000319584.10:c.969C>A	ENSP00000313006.6:p.Ser323Arg
ENST00000346085.9:c.2742C>A	ENSP00000344546.4:p.Ser914Arg
ENST00000350026.9:c.2703C>A	ENSP00000055163.7:p.Ser901Arg
ENST00000414678.6:c.1110C>A	ENSP00000412835.2:p.Ser370Arg
ENST00000452544.1:n.799C>A
ENST00000478761.3:c.25C>A
NM_017519.2:c.2703C>A	NP_059989.2:p.Ser901Arg
NM_020732.3:c.2742C>A	NP_065783.3:p.Ser914Arg
XM_005267069.3:c.2703C>A	XP_005267126.2:p.Ser901Arg
XM_011535984.1:c.1653C>A	XP_011534286.1:p.Ser551Arg
XM_011535985.1:c.1473C>A	XP_011534287.1:p.Ser491Arg
XM_011535986.1:c.1233C>A	XP_011534288.1:p.Ser411Arg
XM_011535987.1:c.852C>A	XP_011534289.1:p.Ser284Arg
XM_011535988.1:c.-20+15607C>A	XP_011534290.1:n.-20+15607C>A
NM_001346813.1:c.2703C>A	NP_001333742.1:p.Ser901Arg
NM_001363725.1:c.453C>A	NP_001350654.1:p.Ser151Arg
XM_011535984.2:c.2784C>A	XP_011534286.2:p.Ser928Arg
XM_011535988.3:c.-20+15607C>A	XP_011534290.1:n.-20+15607C>A
XM_017011103.2:c.2784C>A	XP_016866592.1:p.Ser928Arg
XM_017011104.1:c.2784C>A	XP_016866593.1:p.Ser928Arg
XM_017011105.2:c.2784C>A	XP_016866594.1:p.Ser928Arg
XM_017011106.2:c.2784C>A	XP_016866595.1:p.Ser928Arg
XM_017011107.2:c.2604C>A	XP_016866596.1:p.Ser868Arg
XR_002956289.1:n.2867C>A
NM_001363725.2:c.453C>A	NP_001350654.1:p.Ser151Arg
NM_001371656.1:c.2991C>A	NP_001358585.1:p.Ser997Arg
NM_001374820.1:c.2991C>A	NP_001361749.1:p.Ser997Arg
NM_001374828.1:c.2952C>A MANE Select	NP_001361757.1:p.Ser984Arg
NM_017519.3:c.2952C>A	NP_059989.3:p.Ser984Arg