Canonical Allele Identifier: CA366388981

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469934C>T (hg19) ; chr6:g.157148800C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148800C>T , CM000668.2:g.157148800C>T	GRCh38
NC_000006.11:g.157469934C>T , CM000668.1:g.157469934C>T	GRCh37
NC_000006.10:g.157511626C>T	NCBI36
NG_032093.1:g.375871C>T
NG_032093.2:g.375871C>T
NG_066624.1:g.377775C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2938C>T	ENSP00000055163.8:p.Pro980Ser
ENST00000414678.8:c.2848C>T	ENSP00000412835.3:p.Pro950Ser
ENST00000637015.2:c.2938C>T	ENSP00000489729.2:p.Pro980Ser
ENST00000319584.11:c.952C>T	ENSP00000313006.7:p.Pro318Ser
ENST00000346085.10:c.2977C>T	ENSP00000344546.5:p.Pro993Ser
ENST00000350026.10:c.2689C>T	ENSP00000055163.7:p.Pro897Ser
ENST00000414678.7:c.1096C>T	ENSP00000412835.2:p.Pro366Ser
ENST00000452544.2:n.839C>T
ENST00000635849.1:c.259C>T	ENSP00000490948.1:p.Pro87Ser
ENST00000636426.1:n.72C>T
ENST00000636930.2:c.2938C>T MANE Select	ENSP00000490491.2:p.Pro980Ser
ENST00000637015.1:c.177C>T
ENST00000637810.1:c.439C>T	ENSP00000489636.1:p.Pro147Ser
ENST00000637904.1:c.439C>T	ENSP00000490550.1:p.Pro147Ser
ENST00000647938.1:c.2728C>T	ENSP00000498155.1:p.Pro910Ser
ENST00000674190.1:n.1687C>T
ENST00000319584.10:c.955C>T	ENSP00000313006.6:p.Pro319Ser
ENST00000346085.9:c.2728C>T	ENSP00000344546.4:p.Pro910Ser
ENST00000350026.9:c.2689C>T	ENSP00000055163.7:p.Pro897Ser
ENST00000414678.6:c.1096C>T	ENSP00000412835.2:p.Pro366Ser
ENST00000452544.1:n.785C>T
ENST00000478761.3:c.11C>T
NM_017519.2:c.2689C>T	NP_059989.2:p.Pro897Ser
NM_020732.3:c.2728C>T	NP_065783.3:p.Pro910Ser
XM_005267069.3:c.2689C>T	XP_005267126.2:p.Pro897Ser
XM_011535984.1:c.1639C>T	XP_011534286.1:p.Pro547Ser
XM_011535985.1:c.1459C>T	XP_011534287.1:p.Pro487Ser
XM_011535986.1:c.1219C>T	XP_011534288.1:p.Pro407Ser
XM_011535987.1:c.838C>T	XP_011534289.1:p.Pro280Ser
XM_011535988.1:c.-20+15593C>T	XP_011534290.1:n.-20+15593C>T
NM_001346813.1:c.2689C>T	NP_001333742.1:p.Pro897Ser
NM_001363725.1:c.439C>T	NP_001350654.1:p.Pro147Ser
XM_011535984.2:c.2770C>T	XP_011534286.2:p.Pro924Ser
XM_011535988.3:c.-20+15593C>T	XP_011534290.1:n.-20+15593C>T
XM_017011103.2:c.2770C>T	XP_016866592.1:p.Pro924Ser
XM_017011104.1:c.2770C>T	XP_016866593.1:p.Pro924Ser
XM_017011105.2:c.2770C>T	XP_016866594.1:p.Pro924Ser
XM_017011106.2:c.2770C>T	XP_016866595.1:p.Pro924Ser
XM_017011107.2:c.2590C>T	XP_016866596.1:p.Pro864Ser
XR_002956289.1:n.2853C>T
NM_001363725.2:c.439C>T	NP_001350654.1:p.Pro147Ser
NM_001371656.1:c.2977C>T	NP_001358585.1:p.Pro993Ser
NM_001374820.1:c.2977C>T	NP_001361749.1:p.Pro993Ser
NM_001374828.1:c.2938C>T MANE Select	NP_001361757.1:p.Pro980Ser
NM_017519.3:c.2938C>T	NP_059989.3:p.Pro980Ser