Canonical Allele Identifier: CA366389027

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2127170
• ClinVar RCV Id: RCV003052028
• MyVariant Identifiers: chr6:g.157469953T>C (hg19) ; chr6:g.157148819T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148819T>C , CM000668.2:g.157148819T>C	GRCh38
NC_000006.11:g.157469953T>C , CM000668.1:g.157469953T>C	GRCh37
NC_000006.10:g.157511645T>C	NCBI36
NG_032093.1:g.375890T>C
NG_032093.2:g.375890T>C
NG_066624.1:g.377794T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2957T>C	ENSP00000055163.8:p.Met986Thr
ENST00000414678.8:c.2867T>C	ENSP00000412835.3:p.Met956Thr
ENST00000637015.2:c.2957T>C	ENSP00000489729.2:p.Met986Thr
ENST00000319584.11:c.971T>C	ENSP00000313006.7:p.Met324Thr
ENST00000346085.10:c.2996T>C	ENSP00000344546.5:p.Met999Thr
ENST00000350026.10:c.2708T>C	ENSP00000055163.7:p.Met903Thr
ENST00000414678.7:c.1115T>C	ENSP00000412835.2:p.Met372Thr
ENST00000452544.2:n.858T>C
ENST00000635849.1:c.278T>C	ENSP00000490948.1:p.Met93Thr
ENST00000636426.1:n.91T>C
ENST00000636930.2:c.2957T>C MANE Select	ENSP00000490491.2:p.Met986Thr
ENST00000637015.1:c.196T>C
ENST00000637810.1:c.458T>C	ENSP00000489636.1:p.Met153Thr
ENST00000637904.1:c.458T>C	ENSP00000490550.1:p.Met153Thr
ENST00000647938.1:c.2747T>C	ENSP00000498155.1:p.Met916Thr
ENST00000674190.1:n.1706T>C
ENST00000319584.10:c.974T>C	ENSP00000313006.6:p.Met325Thr
ENST00000346085.9:c.2747T>C	ENSP00000344546.4:p.Met916Thr
ENST00000350026.9:c.2708T>C	ENSP00000055163.7:p.Met903Thr
ENST00000414678.6:c.1115T>C	ENSP00000412835.2:p.Met372Thr
ENST00000452544.1:n.804T>C
ENST00000478761.3:c.30T>C
NM_017519.2:c.2708T>C	NP_059989.2:p.Met903Thr
NM_020732.3:c.2747T>C	NP_065783.3:p.Met916Thr
XM_005267069.3:c.2708T>C	XP_005267126.2:p.Met903Thr
XM_011535984.1:c.1658T>C	XP_011534286.1:p.Met553Thr
XM_011535985.1:c.1478T>C	XP_011534287.1:p.Met493Thr
XM_011535986.1:c.1238T>C	XP_011534288.1:p.Met413Thr
XM_011535987.1:c.857T>C	XP_011534289.1:p.Met286Thr
XM_011535988.1:c.-20+15612T>C	XP_011534290.1:n.-20+15612T>C
NM_001346813.1:c.2708T>C	NP_001333742.1:p.Met903Thr
NM_001363725.1:c.458T>C	NP_001350654.1:p.Met153Thr
XM_011535984.2:c.2789T>C	XP_011534286.2:p.Met930Thr
XM_011535988.3:c.-20+15612T>C	XP_011534290.1:n.-20+15612T>C
XM_017011103.2:c.2789T>C	XP_016866592.1:p.Met930Thr
XM_017011104.1:c.2789T>C	XP_016866593.1:p.Met930Thr
XM_017011105.2:c.2789T>C	XP_016866594.1:p.Met930Thr
XM_017011106.2:c.2789T>C	XP_016866595.1:p.Met930Thr
XM_017011107.2:c.2609T>C	XP_016866596.1:p.Met870Thr
XR_002956289.1:n.2872T>C
NM_001363725.2:c.458T>C	NP_001350654.1:p.Met153Thr
NM_001371656.1:c.2996T>C	NP_001358585.1:p.Met999Thr
NM_001374820.1:c.2996T>C	NP_001361749.1:p.Met999Thr
NM_001374828.1:c.2957T>C MANE Select	NP_001361757.1:p.Met986Thr
NM_017519.3:c.2957T>C	NP_059989.3:p.Met986Thr