Canonical Allele Identifier: CA452990156

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470083C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148949C>T , CM000668.2:g.157148949C>T	GRCh38
NC_000006.11:g.157470083C>T , CM000668.1:g.157470083C>T	GRCh37
NC_000006.10:g.157511775C>T	NCBI36
NG_032093.1:g.376020C>T
NG_032093.2:g.376020C>T
NG_066624.1:g.377924C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3087C>T	ENSP00000055163.8:p.Ser1029=
ENST00000414678.8:c.2997C>T	ENSP00000412835.3:p.Ser999=
ENST00000637015.2:c.3087C>T	ENSP00000489729.2:p.Ser1029=
ENST00000319584.11:c.1101C>T	ENSP00000313006.7:p.Ser367=
ENST00000346085.10:c.3126C>T	ENSP00000344546.5:p.Ser1042=
ENST00000350026.10:c.2838C>T	ENSP00000055163.7:p.Ser946=
ENST00000414678.7:c.1245C>T	ENSP00000412835.2:p.Ser415=
ENST00000452544.2:n.988C>T
ENST00000635849.1:c.408C>T	ENSP00000490948.1:p.Ser136=
ENST00000635957.1:c.42C>T	ENSP00000490385.1:p.Ser14=
ENST00000636426.1:n.221C>T
ENST00000636930.2:c.3087C>T MANE Select	ENSP00000490491.2:p.Ser1029=
ENST00000637015.1:c.326C>T
ENST00000637568.1:c.130C>T
ENST00000637810.1:c.588C>T	ENSP00000489636.1:p.Ser196=
ENST00000637904.1:c.588C>T	ENSP00000490550.1:p.Ser196=
ENST00000647938.1:c.2877C>T	ENSP00000498155.1:p.Ser959=
ENST00000674190.1:n.1836C>T
ENST00000319584.10:c.1104C>T	ENSP00000313006.6:p.Ser368=
ENST00000346085.9:c.2877C>T	ENSP00000344546.4:p.Ser959=
ENST00000350026.9:c.2838C>T	ENSP00000055163.7:p.Ser946=
ENST00000400790.3:c.39C>T	ENSP00000383596.3:p.Ser13=
ENST00000414678.6:c.1245C>T	ENSP00000412835.2:p.Ser415=
ENST00000452544.1:n.934C>T
ENST00000478761.3:c.160C>T
NM_017519.2:c.2838C>T	NP_059989.2:p.Ser946=
NM_020732.3:c.2877C>T	NP_065783.3:p.Ser959=
XM_005267069.3:c.2838C>T	XP_005267126.2:p.Ser946=
XM_011535984.1:c.1788C>T	XP_011534286.1:p.Ser596=
XM_011535985.1:c.1608C>T	XP_011534287.1:p.Ser536=
XM_011535986.1:c.1368C>T	XP_011534288.1:p.Ser456=
XM_011535987.1:c.987C>T	XP_011534289.1:p.Ser329=
XM_011535988.1:c.-20+15742C>T	XP_011534290.1:n.-20+15742C>T
NM_001346813.1:c.2838C>T	NP_001333742.1:p.Ser946=
NM_001363725.1:c.588C>T	NP_001350654.1:p.Ser196=
XM_011535984.2:c.2919C>T	XP_011534286.2:p.Ser973=
XM_011535988.3:c.-20+15742C>T	XP_011534290.1:n.-20+15742C>T
XM_017011103.2:c.2919C>T	XP_016866592.1:p.Ser973=
XM_017011104.1:c.2919C>T	XP_016866593.1:p.Ser973=
XM_017011105.2:c.2919C>T	XP_016866594.1:p.Ser973=
XM_017011106.2:c.2919C>T	XP_016866595.1:p.Ser973=
XM_017011107.2:c.2739C>T	XP_016866596.1:p.Ser913=
XR_002956289.1:n.3002C>T
NM_001363725.2:c.588C>T	NP_001350654.1:p.Ser196=
NM_001371656.1:c.3126C>T	NP_001358585.1:p.Ser1042=
NM_001374820.1:c.3126C>T	NP_001361749.1:p.Ser1042=
NM_001374828.1:c.3087C>T MANE Select	NP_001361757.1:p.Ser1029=
NM_017519.3:c.3087C>T	NP_059989.3:p.Ser1029=