Canonical Allele Identifier: CA366389053

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469964T>C (hg19) ; chr6:g.157148830T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148830T>C , CM000668.2:g.157148830T>C	GRCh38
NC_000006.11:g.157469964T>C , CM000668.1:g.157469964T>C	GRCh37
NC_000006.10:g.157511656T>C	NCBI36
NG_032093.1:g.375901T>C
NG_032093.2:g.375901T>C
NG_066624.1:g.377805T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2968T>C	ENSP00000055163.8:p.Ser990Pro
ENST00000414678.8:c.2878T>C	ENSP00000412835.3:p.Ser960Pro
ENST00000637015.2:c.2968T>C	ENSP00000489729.2:p.Ser990Pro
ENST00000319584.11:c.982T>C	ENSP00000313006.7:p.Ser328Pro
ENST00000346085.10:c.3007T>C	ENSP00000344546.5:p.Ser1003Pro
ENST00000350026.10:c.2719T>C	ENSP00000055163.7:p.Ser907Pro
ENST00000414678.7:c.1126T>C	ENSP00000412835.2:p.Ser376Pro
ENST00000452544.2:n.869T>C
ENST00000635849.1:c.289T>C	ENSP00000490948.1:p.Ser97Pro
ENST00000636426.1:n.102T>C
ENST00000636930.2:c.2968T>C MANE Select	ENSP00000490491.2:p.Ser990Pro
ENST00000637015.1:c.207T>C
ENST00000637568.1:c.11T>C
ENST00000637810.1:c.469T>C	ENSP00000489636.1:p.Ser157Pro
ENST00000637904.1:c.469T>C	ENSP00000490550.1:p.Ser157Pro
ENST00000647938.1:c.2758T>C	ENSP00000498155.1:p.Ser920Pro
ENST00000674190.1:n.1717T>C
ENST00000319584.10:c.985T>C	ENSP00000313006.6:p.Ser329Pro
ENST00000346085.9:c.2758T>C	ENSP00000344546.4:p.Ser920Pro
ENST00000350026.9:c.2719T>C	ENSP00000055163.7:p.Ser907Pro
ENST00000414678.6:c.1126T>C	ENSP00000412835.2:p.Ser376Pro
ENST00000452544.1:n.815T>C
ENST00000478761.3:c.41T>C
NM_017519.2:c.2719T>C	NP_059989.2:p.Ser907Pro
NM_020732.3:c.2758T>C	NP_065783.3:p.Ser920Pro
XM_005267069.3:c.2719T>C	XP_005267126.2:p.Ser907Pro
XM_011535984.1:c.1669T>C	XP_011534286.1:p.Ser557Pro
XM_011535985.1:c.1489T>C	XP_011534287.1:p.Ser497Pro
XM_011535986.1:c.1249T>C	XP_011534288.1:p.Ser417Pro
XM_011535987.1:c.868T>C	XP_011534289.1:p.Ser290Pro
XM_011535988.1:c.-20+15623T>C	XP_011534290.1:n.-20+15623T>C
NM_001346813.1:c.2719T>C	NP_001333742.1:p.Ser907Pro
NM_001363725.1:c.469T>C	NP_001350654.1:p.Ser157Pro
XM_011535984.2:c.2800T>C	XP_011534286.2:p.Ser934Pro
XM_011535988.3:c.-20+15623T>C	XP_011534290.1:n.-20+15623T>C
XM_017011103.2:c.2800T>C	XP_016866592.1:p.Ser934Pro
XM_017011104.1:c.2800T>C	XP_016866593.1:p.Ser934Pro
XM_017011105.2:c.2800T>C	XP_016866594.1:p.Ser934Pro
XM_017011106.2:c.2800T>C	XP_016866595.1:p.Ser934Pro
XM_017011107.2:c.2620T>C	XP_016866596.1:p.Ser874Pro
XR_002956289.1:n.2883T>C
NM_001363725.2:c.469T>C	NP_001350654.1:p.Ser157Pro
NM_001371656.1:c.3007T>C	NP_001358585.1:p.Ser1003Pro
NM_001374820.1:c.3007T>C	NP_001361749.1:p.Ser1003Pro
NM_001374828.1:c.2968T>C MANE Select	NP_001361757.1:p.Ser990Pro
NM_017519.3:c.2968T>C	NP_059989.3:p.Ser990Pro