Canonical Allele Identifier: CA366389234

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3053C>G	ENSP00000055163.8:p.Ala1018Gly
ENST00000414678.8:c.2963C>G	ENSP00000412835.3:p.Ala988Gly
ENST00000637015.2:c.3053C>G	ENSP00000489729.2:p.Ala1018Gly
ENST00000319584.11:c.1067C>G	ENSP00000313006.7:p.Ala356Gly
ENST00000346085.10:c.3092C>G	ENSP00000344546.5:p.Ala1031Gly
ENST00000350026.10:c.2804C>G	ENSP00000055163.7:p.Ala935Gly
ENST00000414678.7:c.1211C>G	ENSP00000412835.2:p.Ala404Gly
ENST00000452544.2:n.954C>G
ENST00000635849.1:c.374C>G	ENSP00000490948.1:p.Ala125Gly
ENST00000635957.1:c.8C>G	ENSP00000490385.1:p.Ala3Gly
ENST00000636426.1:n.187C>G
ENST00000636930.2:c.3053C>G MANE Select	ENSP00000490491.2:p.Ala1018Gly
ENST00000637015.1:c.292C>G
ENST00000637568.1:c.96C>G
ENST00000637810.1:c.554C>G	ENSP00000489636.1:p.Ala185Gly
ENST00000637904.1:c.554C>G	ENSP00000490550.1:p.Ala185Gly
ENST00000647938.1:c.2843C>G	ENSP00000498155.1:p.Ala948Gly
ENST00000674190.1:n.1802C>G
ENST00000319584.10:c.1070C>G	ENSP00000313006.6:p.Ala357Gly
ENST00000346085.9:c.2843C>G	ENSP00000344546.4:p.Ala948Gly
ENST00000350026.9:c.2804C>G	ENSP00000055163.7:p.Ala935Gly
ENST00000400790.3:c.5C>G	ENSP00000383596.3:p.Ala2Gly
ENST00000414678.6:c.1211C>G	ENSP00000412835.2:p.Ala404Gly
ENST00000452544.1:n.900C>G
ENST00000478761.3:c.126C>G
NM_017519.2:c.2804C>G	NP_059989.2:p.Ala935Gly
NM_020732.3:c.2843C>G	NP_065783.3:p.Ala948Gly
XM_005267069.3:c.2804C>G	XP_005267126.2:p.Ala935Gly
XM_011535984.1:c.1754C>G	XP_011534286.1:p.Ala585Gly
XM_011535985.1:c.1574C>G	XP_011534287.1:p.Ala525Gly
XM_011535986.1:c.1334C>G	XP_011534288.1:p.Ala445Gly
XM_011535987.1:c.953C>G	XP_011534289.1:p.Ala318Gly
XM_011535988.1:c.-20+15708C>G	XP_011534290.1:n.-20+15708C>G
NM_001346813.1:c.2804C>G	NP_001333742.1:p.Ala935Gly
NM_001363725.1:c.554C>G	NP_001350654.1:p.Ala185Gly
XM_011535984.2:c.2885C>G	XP_011534286.2:p.Ala962Gly
XM_011535988.3:c.-20+15708C>G	XP_011534290.1:n.-20+15708C>G
XM_017011103.2:c.2885C>G	XP_016866592.1:p.Ala962Gly
XM_017011104.1:c.2885C>G	XP_016866593.1:p.Ala962Gly
XM_017011105.2:c.2885C>G	XP_016866594.1:p.Ala962Gly
XM_017011106.2:c.2885C>G	XP_016866595.1:p.Ala962Gly
XM_017011107.2:c.2705C>G	XP_016866596.1:p.Ala902Gly
XR_002956289.1:n.2968C>G
NM_001363725.2:c.554C>G	NP_001350654.1:p.Ala185Gly
NM_001371656.1:c.3092C>G	NP_001358585.1:p.Ala1031Gly
NM_001374820.1:c.3092C>G	NP_001361749.1:p.Ala1031Gly
NM_001374828.1:c.3053C>G MANE Select	NP_001361757.1:p.Ala1018Gly
NM_017519.3:c.3053C>G	NP_059989.3:p.Ala1018Gly