Canonical Allele Identifier: CA366389186

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470028A>C (hg19) ; chr6:g.157148894A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148894A>C , CM000668.2:g.157148894A>C	GRCh38
NC_000006.11:g.157470028A>C , CM000668.1:g.157470028A>C	GRCh37
NC_000006.10:g.157511720A>C	NCBI36
NG_032093.1:g.375965A>C
NG_032093.2:g.375965A>C
NG_066624.1:g.377869A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3032A>C	ENSP00000055163.8:p.Lys1011Thr
ENST00000414678.8:c.2942A>C	ENSP00000412835.3:p.Lys981Thr
ENST00000637015.2:c.3032A>C	ENSP00000489729.2:p.Lys1011Thr
ENST00000319584.11:c.1046A>C	ENSP00000313006.7:p.Lys349Thr
ENST00000346085.10:c.3071A>C	ENSP00000344546.5:p.Lys1024Thr
ENST00000350026.10:c.2783A>C	ENSP00000055163.7:p.Lys928Thr
ENST00000414678.7:c.1190A>C	ENSP00000412835.2:p.Lys397Thr
ENST00000452544.2:n.933A>C
ENST00000635849.1:c.353A>C	ENSP00000490948.1:p.Lys118Thr
ENST00000636426.1:n.166A>C
ENST00000636930.2:c.3032A>C MANE Select	ENSP00000490491.2:p.Lys1011Thr
ENST00000637015.1:c.271A>C
ENST00000637568.1:c.75A>C
ENST00000637810.1:c.533A>C	ENSP00000489636.1:p.Lys178Thr
ENST00000637904.1:c.533A>C	ENSP00000490550.1:p.Lys178Thr
ENST00000647938.1:c.2822A>C	ENSP00000498155.1:p.Lys941Thr
ENST00000674190.1:n.1781A>C
ENST00000319584.10:c.1049A>C	ENSP00000313006.6:p.Lys350Thr
ENST00000346085.9:c.2822A>C	ENSP00000344546.4:p.Lys941Thr
ENST00000350026.9:c.2783A>C	ENSP00000055163.7:p.Lys928Thr
ENST00000414678.6:c.1190A>C	ENSP00000412835.2:p.Lys397Thr
ENST00000452544.1:n.879A>C
ENST00000478761.3:c.105A>C
NM_017519.2:c.2783A>C	NP_059989.2:p.Lys928Thr
NM_020732.3:c.2822A>C	NP_065783.3:p.Lys941Thr
XM_005267069.3:c.2783A>C	XP_005267126.2:p.Lys928Thr
XM_011535984.1:c.1733A>C	XP_011534286.1:p.Lys578Thr
XM_011535985.1:c.1553A>C	XP_011534287.1:p.Lys518Thr
XM_011535986.1:c.1313A>C	XP_011534288.1:p.Lys438Thr
XM_011535987.1:c.932A>C	XP_011534289.1:p.Lys311Thr
XM_011535988.1:c.-20+15687A>C	XP_011534290.1:n.-20+15687A>C
NM_001346813.1:c.2783A>C	NP_001333742.1:p.Lys928Thr
NM_001363725.1:c.533A>C	NP_001350654.1:p.Lys178Thr
XM_011535984.2:c.2864A>C	XP_011534286.2:p.Lys955Thr
XM_011535988.3:c.-20+15687A>C	XP_011534290.1:n.-20+15687A>C
XM_017011103.2:c.2864A>C	XP_016866592.1:p.Lys955Thr
XM_017011104.1:c.2864A>C	XP_016866593.1:p.Lys955Thr
XM_017011105.2:c.2864A>C	XP_016866594.1:p.Lys955Thr
XM_017011106.2:c.2864A>C	XP_016866595.1:p.Lys955Thr
XM_017011107.2:c.2684A>C	XP_016866596.1:p.Lys895Thr
XR_002956289.1:n.2947A>C
NM_001363725.2:c.533A>C	NP_001350654.1:p.Lys178Thr
NM_001371656.1:c.3071A>C	NP_001358585.1:p.Lys1024Thr
NM_001374820.1:c.3071A>C	NP_001361749.1:p.Lys1024Thr
NM_001374828.1:c.3032A>C MANE Select	NP_001361757.1:p.Lys1011Thr
NM_017519.3:c.3032A>C	NP_059989.3:p.Lys1011Thr