Canonical Allele Identifier: CA366389284

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470073C>T (hg19) ; chr6:g.157148939C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148939C>T , CM000668.2:g.157148939C>T	GRCh38
NC_000006.11:g.157470073C>T , CM000668.1:g.157470073C>T	GRCh37
NC_000006.10:g.157511765C>T	NCBI36
NG_032093.1:g.376010C>T
NG_032093.2:g.376010C>T
NG_066624.1:g.377914C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3077C>T	ENSP00000055163.8:p.Ser1026Leu
ENST00000414678.8:c.2987C>T	ENSP00000412835.3:p.Ser996Leu
ENST00000637015.2:c.3077C>T	ENSP00000489729.2:p.Ser1026Leu
ENST00000319584.11:c.1091C>T	ENSP00000313006.7:p.Ser364Leu
ENST00000346085.10:c.3116C>T	ENSP00000344546.5:p.Ser1039Leu
ENST00000350026.10:c.2828C>T	ENSP00000055163.7:p.Ser943Leu
ENST00000414678.7:c.1235C>T	ENSP00000412835.2:p.Ser412Leu
ENST00000452544.2:n.978C>T
ENST00000635849.1:c.398C>T	ENSP00000490948.1:p.Ser133Leu
ENST00000635957.1:c.32C>T	ENSP00000490385.1:p.Ser11Leu
ENST00000636426.1:n.211C>T
ENST00000636930.2:c.3077C>T MANE Select	ENSP00000490491.2:p.Ser1026Leu
ENST00000637015.1:c.316C>T
ENST00000637568.1:c.120C>T
ENST00000637810.1:c.578C>T	ENSP00000489636.1:p.Ser193Leu
ENST00000637904.1:c.578C>T	ENSP00000490550.1:p.Ser193Leu
ENST00000647938.1:c.2867C>T	ENSP00000498155.1:p.Ser956Leu
ENST00000674190.1:n.1826C>T
ENST00000319584.10:c.1094C>T	ENSP00000313006.6:p.Ser365Leu
ENST00000346085.9:c.2867C>T	ENSP00000344546.4:p.Ser956Leu
ENST00000350026.9:c.2828C>T	ENSP00000055163.7:p.Ser943Leu
ENST00000400790.3:c.29C>T	ENSP00000383596.3:p.Ser10Leu
ENST00000414678.6:c.1235C>T	ENSP00000412835.2:p.Ser412Leu
ENST00000452544.1:n.924C>T
ENST00000478761.3:c.150C>T
NM_017519.2:c.2828C>T	NP_059989.2:p.Ser943Leu
NM_020732.3:c.2867C>T	NP_065783.3:p.Ser956Leu
XM_005267069.3:c.2828C>T	XP_005267126.2:p.Ser943Leu
XM_011535984.1:c.1778C>T	XP_011534286.1:p.Ser593Leu
XM_011535985.1:c.1598C>T	XP_011534287.1:p.Ser533Leu
XM_011535986.1:c.1358C>T	XP_011534288.1:p.Ser453Leu
XM_011535987.1:c.977C>T	XP_011534289.1:p.Ser326Leu
XM_011535988.1:c.-20+15732C>T	XP_011534290.1:n.-20+15732C>T
NM_001346813.1:c.2828C>T	NP_001333742.1:p.Ser943Leu
NM_001363725.1:c.578C>T	NP_001350654.1:p.Ser193Leu
XM_011535984.2:c.2909C>T	XP_011534286.2:p.Ser970Leu
XM_011535988.3:c.-20+15732C>T	XP_011534290.1:n.-20+15732C>T
XM_017011103.2:c.2909C>T	XP_016866592.1:p.Ser970Leu
XM_017011104.1:c.2909C>T	XP_016866593.1:p.Ser970Leu
XM_017011105.2:c.2909C>T	XP_016866594.1:p.Ser970Leu
XM_017011106.2:c.2909C>T	XP_016866595.1:p.Ser970Leu
XM_017011107.2:c.2729C>T	XP_016866596.1:p.Ser910Leu
XR_002956289.1:n.2992C>T
NM_001363725.2:c.578C>T	NP_001350654.1:p.Ser193Leu
NM_001371656.1:c.3116C>T	NP_001358585.1:p.Ser1039Leu
NM_001374820.1:c.3116C>T	NP_001361749.1:p.Ser1039Leu
NM_001374828.1:c.3077C>T MANE Select	NP_001361757.1:p.Ser1026Leu
NM_017519.3:c.3077C>T	NP_059989.3:p.Ser1026Leu