Canonical Allele Identifier: CA366389235

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470049C>A (hg19) ; chr6:g.157148915C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148915C>A , CM000668.2:g.157148915C>A	GRCh38
NC_000006.11:g.157470049C>A , CM000668.1:g.157470049C>A	GRCh37
NC_000006.10:g.157511741C>A	NCBI36
NG_032093.1:g.375986C>A
NG_032093.2:g.375986C>A
NG_066624.1:g.377890C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3053C>A	ENSP00000055163.8:p.Ala1018Glu
ENST00000414678.8:c.2963C>A	ENSP00000412835.3:p.Ala988Glu
ENST00000637015.2:c.3053C>A	ENSP00000489729.2:p.Ala1018Glu
ENST00000319584.11:c.1067C>A	ENSP00000313006.7:p.Ala356Glu
ENST00000346085.10:c.3092C>A	ENSP00000344546.5:p.Ala1031Glu
ENST00000350026.10:c.2804C>A	ENSP00000055163.7:p.Ala935Glu
ENST00000414678.7:c.1211C>A	ENSP00000412835.2:p.Ala404Glu
ENST00000452544.2:n.954C>A
ENST00000635849.1:c.374C>A	ENSP00000490948.1:p.Ala125Glu
ENST00000635957.1:c.8C>A	ENSP00000490385.1:p.Ala3Glu
ENST00000636426.1:n.187C>A
ENST00000636930.2:c.3053C>A MANE Select	ENSP00000490491.2:p.Ala1018Glu
ENST00000637015.1:c.292C>A
ENST00000637568.1:c.96C>A
ENST00000637810.1:c.554C>A	ENSP00000489636.1:p.Ala185Glu
ENST00000637904.1:c.554C>A	ENSP00000490550.1:p.Ala185Glu
ENST00000647938.1:c.2843C>A	ENSP00000498155.1:p.Ala948Glu
ENST00000674190.1:n.1802C>A
ENST00000319584.10:c.1070C>A	ENSP00000313006.6:p.Ala357Glu
ENST00000346085.9:c.2843C>A	ENSP00000344546.4:p.Ala948Glu
ENST00000350026.9:c.2804C>A	ENSP00000055163.7:p.Ala935Glu
ENST00000400790.3:c.5C>A	ENSP00000383596.3:p.Ala2Glu
ENST00000414678.6:c.1211C>A	ENSP00000412835.2:p.Ala404Glu
ENST00000452544.1:n.900C>A
ENST00000478761.3:c.126C>A
NM_017519.2:c.2804C>A	NP_059989.2:p.Ala935Glu
NM_020732.3:c.2843C>A	NP_065783.3:p.Ala948Glu
XM_005267069.3:c.2804C>A	XP_005267126.2:p.Ala935Glu
XM_011535984.1:c.1754C>A	XP_011534286.1:p.Ala585Glu
XM_011535985.1:c.1574C>A	XP_011534287.1:p.Ala525Glu
XM_011535986.1:c.1334C>A	XP_011534288.1:p.Ala445Glu
XM_011535987.1:c.953C>A	XP_011534289.1:p.Ala318Glu
XM_011535988.1:c.-20+15708C>A	XP_011534290.1:n.-20+15708C>A
NM_001346813.1:c.2804C>A	NP_001333742.1:p.Ala935Glu
NM_001363725.1:c.554C>A	NP_001350654.1:p.Ala185Glu
XM_011535984.2:c.2885C>A	XP_011534286.2:p.Ala962Glu
XM_011535988.3:c.-20+15708C>A	XP_011534290.1:n.-20+15708C>A
XM_017011103.2:c.2885C>A	XP_016866592.1:p.Ala962Glu
XM_017011104.1:c.2885C>A	XP_016866593.1:p.Ala962Glu
XM_017011105.2:c.2885C>A	XP_016866594.1:p.Ala962Glu
XM_017011106.2:c.2885C>A	XP_016866595.1:p.Ala962Glu
XM_017011107.2:c.2705C>A	XP_016866596.1:p.Ala902Glu
XR_002956289.1:n.2968C>A
NM_001363725.2:c.554C>A	NP_001350654.1:p.Ala185Glu
NM_001371656.1:c.3092C>A	NP_001358585.1:p.Ala1031Glu
NM_001374820.1:c.3092C>A	NP_001361749.1:p.Ala1031Glu
NM_001374828.1:c.3053C>A MANE Select	NP_001361757.1:p.Ala1018Glu
NM_017519.3:c.3053C>A	NP_059989.3:p.Ala1018Glu