Canonical Allele Identifier: CA366388976

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469932T>C (hg19) ; chr6:g.157148798T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148798T>C , CM000668.2:g.157148798T>C	GRCh38
NC_000006.11:g.157469932T>C , CM000668.1:g.157469932T>C	GRCh37
NC_000006.10:g.157511624T>C	NCBI36
NG_032093.1:g.375869T>C
NG_032093.2:g.375869T>C
NG_066624.1:g.377773T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2936T>C	ENSP00000055163.8:p.Phe979Ser
ENST00000414678.8:c.2846T>C	ENSP00000412835.3:p.Phe949Ser
ENST00000637015.2:c.2936T>C	ENSP00000489729.2:p.Phe979Ser
ENST00000319584.11:c.950T>C	ENSP00000313006.7:p.Phe317Ser
ENST00000346085.10:c.2975T>C	ENSP00000344546.5:p.Phe992Ser
ENST00000350026.10:c.2687T>C	ENSP00000055163.7:p.Phe896Ser
ENST00000414678.7:c.1094T>C	ENSP00000412835.2:p.Phe365Ser
ENST00000452544.2:n.837T>C
ENST00000635849.1:c.257T>C	ENSP00000490948.1:p.Phe86Ser
ENST00000636426.1:n.70T>C
ENST00000636930.2:c.2936T>C MANE Select	ENSP00000490491.2:p.Phe979Ser
ENST00000637015.1:c.175T>C
ENST00000637810.1:c.437T>C	ENSP00000489636.1:p.Phe146Ser
ENST00000637904.1:c.437T>C	ENSP00000490550.1:p.Phe146Ser
ENST00000647938.1:c.2726T>C	ENSP00000498155.1:p.Phe909Ser
ENST00000674190.1:n.1685T>C
ENST00000319584.10:c.953T>C	ENSP00000313006.6:p.Phe318Ser
ENST00000346085.9:c.2726T>C	ENSP00000344546.4:p.Phe909Ser
ENST00000350026.9:c.2687T>C	ENSP00000055163.7:p.Phe896Ser
ENST00000414678.6:c.1094T>C	ENSP00000412835.2:p.Phe365Ser
ENST00000452544.1:n.783T>C
ENST00000478761.3:c.9T>C
NM_017519.2:c.2687T>C	NP_059989.2:p.Phe896Ser
NM_020732.3:c.2726T>C	NP_065783.3:p.Phe909Ser
XM_005267069.3:c.2687T>C	XP_005267126.2:p.Phe896Ser
XM_011535984.1:c.1637T>C	XP_011534286.1:p.Phe546Ser
XM_011535985.1:c.1457T>C	XP_011534287.1:p.Phe486Ser
XM_011535986.1:c.1217T>C	XP_011534288.1:p.Phe406Ser
XM_011535987.1:c.836T>C	XP_011534289.1:p.Phe279Ser
XM_011535988.1:c.-20+15591T>C	XP_011534290.1:n.-20+15591T>C
NM_001346813.1:c.2687T>C	NP_001333742.1:p.Phe896Ser
NM_001363725.1:c.437T>C	NP_001350654.1:p.Phe146Ser
XM_011535984.2:c.2768T>C	XP_011534286.2:p.Phe923Ser
XM_011535988.3:c.-20+15591T>C	XP_011534290.1:n.-20+15591T>C
XM_017011103.2:c.2768T>C	XP_016866592.1:p.Phe923Ser
XM_017011104.1:c.2768T>C	XP_016866593.1:p.Phe923Ser
XM_017011105.2:c.2768T>C	XP_016866594.1:p.Phe923Ser
XM_017011106.2:c.2768T>C	XP_016866595.1:p.Phe923Ser
XM_017011107.2:c.2588T>C	XP_016866596.1:p.Phe863Ser
XR_002956289.1:n.2851T>C
NM_001363725.2:c.437T>C	NP_001350654.1:p.Phe146Ser
NM_001371656.1:c.2975T>C	NP_001358585.1:p.Phe992Ser
NM_001374820.1:c.2975T>C	NP_001361749.1:p.Phe992Ser
NM_001374828.1:c.2936T>C MANE Select	NP_001361757.1:p.Phe979Ser
NM_017519.3:c.2936T>C	NP_059989.3:p.Phe979Ser