Canonical Allele Identifier: CA366235285

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511242A>C (hg19) ; chr6:g.157190108A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190108A>C , CM000668.2:g.157190108A>C	GRCh38
NC_000006.11:g.157511242A>C , CM000668.1:g.157511242A>C	GRCh37
NC_000006.10:g.157552934A>C	NCBI36
NG_032093.1:g.417179A>C
NG_032093.2:g.417179A>C
NG_066624.1:g.419083A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3970A>C	ENSP00000055163.8:p.Met1324Leu
ENST00000414678.8:c.4039A>C	ENSP00000412835.3:p.Met1347Leu
ENST00000637015.2:c.4258A>C	ENSP00000489729.2:p.Met1420Leu
ENST00000346085.10:c.4009A>C	ENSP00000344546.5:p.Met1337Leu
ENST00000350026.10:c.3721A>C	ENSP00000055163.7:p.Met1241Leu
ENST00000414678.7:c.2287A>C	ENSP00000412835.2:p.Met763Leu
ENST00000635849.1:c.1450A>C	ENSP00000490948.1:p.Met484Leu
ENST00000635957.1:c.1081A>C	ENSP00000490385.1:p.Met361Leu
ENST00000636930.2:c.4129A>C MANE Select	ENSP00000490491.2:p.Met1377Leu
ENST00000636940.1:n.2126A>C
ENST00000637015.1:c.1497A>C
ENST00000637568.1:c.1411A>C
ENST00000637741.1:n.795A>C
ENST00000637810.1:c.1471A>C	ENSP00000489636.1:p.Met491Leu
ENST00000637904.1:c.1630A>C	ENSP00000490550.1:p.Met544Leu
ENST00000647938.1:c.3760A>C	ENSP00000498155.1:p.Met1254Leu
ENST00000346085.9:c.3760A>C	ENSP00000344546.4:p.Met1254Leu
ENST00000350026.9:c.3721A>C	ENSP00000055163.7:p.Met1241Leu
ENST00000414678.6:c.2287A>C	ENSP00000412835.2:p.Met763Leu
NM_017519.2:c.3721A>C	NP_059989.2:p.Met1241Leu
NM_020732.3:c.3760A>C	NP_065783.3:p.Met1254Leu
XM_005267069.3:c.3880A>C	XP_005267126.2:p.Met1294Leu
XM_011535984.1:c.2959A>C	XP_011534286.1:p.Met987Leu
XM_011535985.1:c.2779A>C	XP_011534287.1:p.Met927Leu
XM_011535986.1:c.2539A>C	XP_011534288.1:p.Met847Leu
XM_011535987.1:c.2158A>C	XP_011534289.1:p.Met720Leu
XM_011535988.1:c.1021A>C	XP_011534290.1:p.Met341Leu
NM_001346813.1:c.3880A>C	NP_001333742.1:p.Met1294Leu
NM_001363725.1:c.1630A>C	NP_001350654.1:p.Met544Leu
XM_011535984.2:c.4090A>C	XP_011534286.2:p.Met1364Leu
XM_011535988.3:c.1021A>C	XP_011534290.1:p.Met341Leu
XM_017011103.2:c.3991A>C	XP_016866592.1:p.Met1331Leu
XM_017011104.1:c.3961A>C	XP_016866593.1:p.Met1321Leu
XM_017011105.2:c.3931A>C	XP_016866594.1:p.Met1311Leu
XM_017011106.2:c.3802A>C	XP_016866595.1:p.Met1268Leu
XM_017011107.2:c.3781A>C	XP_016866596.1:p.Met1261Leu
XR_002956289.1:n.4173A>C
NM_001363725.2:c.1630A>C	NP_001350654.1:p.Met544Leu
NM_001371656.1:c.4009A>C	NP_001358585.1:p.Met1337Leu
NM_001374820.1:c.4009A>C	NP_001361749.1:p.Met1337Leu
NM_001374828.1:c.4129A>C MANE Select	NP_001361757.1:p.Met1377Leu
NM_017519.3:c.3970A>C	NP_059989.3:p.Met1324Leu