Canonical Allele Identifier: CA452990215

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469936T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148802T>C , CM000668.2:g.157148802T>C	GRCh38
NC_000006.11:g.157469936T>C , CM000668.1:g.157469936T>C	GRCh37
NC_000006.10:g.157511628T>C	NCBI36
NG_032093.1:g.375873T>C
NG_032093.2:g.375873T>C
NG_066624.1:g.377777T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2940T>C	ENSP00000055163.8:p.Pro980=
ENST00000414678.8:c.2850T>C	ENSP00000412835.3:p.Pro950=
ENST00000637015.2:c.2940T>C	ENSP00000489729.2:p.Pro980=
ENST00000319584.11:c.954T>C	ENSP00000313006.7:p.Pro318=
ENST00000346085.10:c.2979T>C	ENSP00000344546.5:p.Pro993=
ENST00000350026.10:c.2691T>C	ENSP00000055163.7:p.Pro897=
ENST00000414678.7:c.1098T>C	ENSP00000412835.2:p.Pro366=
ENST00000452544.2:n.841T>C
ENST00000635849.1:c.261T>C	ENSP00000490948.1:p.Pro87=
ENST00000636426.1:n.74T>C
ENST00000636930.2:c.2940T>C MANE Select	ENSP00000490491.2:p.Pro980=
ENST00000637015.1:c.179T>C
ENST00000637810.1:c.441T>C	ENSP00000489636.1:p.Pro147=
ENST00000637904.1:c.441T>C	ENSP00000490550.1:p.Pro147=
ENST00000647938.1:c.2730T>C	ENSP00000498155.1:p.Pro910=
ENST00000674190.1:n.1689T>C
ENST00000319584.10:c.957T>C	ENSP00000313006.6:p.Pro319=
ENST00000346085.9:c.2730T>C	ENSP00000344546.4:p.Pro910=
ENST00000350026.9:c.2691T>C	ENSP00000055163.7:p.Pro897=
ENST00000414678.6:c.1098T>C	ENSP00000412835.2:p.Pro366=
ENST00000452544.1:n.787T>C
ENST00000478761.3:c.13T>C
NM_017519.2:c.2691T>C	NP_059989.2:p.Pro897=
NM_020732.3:c.2730T>C	NP_065783.3:p.Pro910=
XM_005267069.3:c.2691T>C	XP_005267126.2:p.Pro897=
XM_011535984.1:c.1641T>C	XP_011534286.1:p.Pro547=
XM_011535985.1:c.1461T>C	XP_011534287.1:p.Pro487=
XM_011535986.1:c.1221T>C	XP_011534288.1:p.Pro407=
XM_011535987.1:c.840T>C	XP_011534289.1:p.Pro280=
XM_011535988.1:c.-20+15595T>C	XP_011534290.1:n.-20+15595T>C
NM_001346813.1:c.2691T>C	NP_001333742.1:p.Pro897=
NM_001363725.1:c.441T>C	NP_001350654.1:p.Pro147=
XM_011535984.2:c.2772T>C	XP_011534286.2:p.Pro924=
XM_011535988.3:c.-20+15595T>C	XP_011534290.1:n.-20+15595T>C
XM_017011103.2:c.2772T>C	XP_016866592.1:p.Pro924=
XM_017011104.1:c.2772T>C	XP_016866593.1:p.Pro924=
XM_017011105.2:c.2772T>C	XP_016866594.1:p.Pro924=
XM_017011106.2:c.2772T>C	XP_016866595.1:p.Pro924=
XM_017011107.2:c.2592T>C	XP_016866596.1:p.Pro864=
XR_002956289.1:n.2855T>C
NM_001363725.2:c.441T>C	NP_001350654.1:p.Pro147=
NM_001371656.1:c.2979T>C	NP_001358585.1:p.Pro993=
NM_001374820.1:c.2979T>C	NP_001361749.1:p.Pro993=
NM_001374828.1:c.2940T>C MANE Select	NP_001361757.1:p.Pro980=
NM_017519.3:c.2940T>C	NP_059989.3:p.Pro980=