Canonical Allele Identifier: CA366389227

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470046C>G (hg19) ; chr6:g.157148912C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148912C>G , CM000668.2:g.157148912C>G	GRCh38
NC_000006.11:g.157470046C>G , CM000668.1:g.157470046C>G	GRCh37
NC_000006.10:g.157511738C>G	NCBI36
NG_032093.1:g.375983C>G
NG_032093.2:g.375983C>G
NG_066624.1:g.377887C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3050C>G	ENSP00000055163.8:p.Ala1017Gly
ENST00000414678.8:c.2960C>G	ENSP00000412835.3:p.Ala987Gly
ENST00000637015.2:c.3050C>G	ENSP00000489729.2:p.Ala1017Gly
ENST00000319584.11:c.1064C>G	ENSP00000313006.7:p.Ala355Gly
ENST00000346085.10:c.3089C>G	ENSP00000344546.5:p.Ala1030Gly
ENST00000350026.10:c.2801C>G	ENSP00000055163.7:p.Ala934Gly
ENST00000414678.7:c.1208C>G	ENSP00000412835.2:p.Ala403Gly
ENST00000452544.2:n.951C>G
ENST00000635849.1:c.371C>G	ENSP00000490948.1:p.Ala124Gly
ENST00000635957.1:c.5C>G	ENSP00000490385.1:p.Ala2Gly
ENST00000636426.1:n.184C>G
ENST00000636930.2:c.3050C>G MANE Select	ENSP00000490491.2:p.Ala1017Gly
ENST00000637015.1:c.289C>G
ENST00000637568.1:c.93C>G
ENST00000637810.1:c.551C>G	ENSP00000489636.1:p.Ala184Gly
ENST00000637904.1:c.551C>G	ENSP00000490550.1:p.Ala184Gly
ENST00000647938.1:c.2840C>G	ENSP00000498155.1:p.Ala947Gly
ENST00000674190.1:n.1799C>G
ENST00000319584.10:c.1067C>G	ENSP00000313006.6:p.Ala356Gly
ENST00000346085.9:c.2840C>G	ENSP00000344546.4:p.Ala947Gly
ENST00000350026.9:c.2801C>G	ENSP00000055163.7:p.Ala934Gly
ENST00000400790.3:c.2C>G	ENSP00000383596.3:p.Ala1Gly
ENST00000414678.6:c.1208C>G	ENSP00000412835.2:p.Ala403Gly
ENST00000452544.1:n.897C>G
ENST00000478761.3:c.123C>G
NM_017519.2:c.2801C>G	NP_059989.2:p.Ala934Gly
NM_020732.3:c.2840C>G	NP_065783.3:p.Ala947Gly
XM_005267069.3:c.2801C>G	XP_005267126.2:p.Ala934Gly
XM_011535984.1:c.1751C>G	XP_011534286.1:p.Ala584Gly
XM_011535985.1:c.1571C>G	XP_011534287.1:p.Ala524Gly
XM_011535986.1:c.1331C>G	XP_011534288.1:p.Ala444Gly
XM_011535987.1:c.950C>G	XP_011534289.1:p.Ala317Gly
XM_011535988.1:c.-20+15705C>G	XP_011534290.1:n.-20+15705C>G
NM_001346813.1:c.2801C>G	NP_001333742.1:p.Ala934Gly
NM_001363725.1:c.551C>G	NP_001350654.1:p.Ala184Gly
XM_011535984.2:c.2882C>G	XP_011534286.2:p.Ala961Gly
XM_011535988.3:c.-20+15705C>G	XP_011534290.1:n.-20+15705C>G
XM_017011103.2:c.2882C>G	XP_016866592.1:p.Ala961Gly
XM_017011104.1:c.2882C>G	XP_016866593.1:p.Ala961Gly
XM_017011105.2:c.2882C>G	XP_016866594.1:p.Ala961Gly
XM_017011106.2:c.2882C>G	XP_016866595.1:p.Ala961Gly
XM_017011107.2:c.2702C>G	XP_016866596.1:p.Ala901Gly
XR_002956289.1:n.2965C>G
NM_001363725.2:c.551C>G	NP_001350654.1:p.Ala184Gly
NM_001371656.1:c.3089C>G	NP_001358585.1:p.Ala1030Gly
NM_001374820.1:c.3089C>G	NP_001361749.1:p.Ala1030Gly
NM_001374828.1:c.3050C>G MANE Select	NP_001361757.1:p.Ala1017Gly
NM_017519.3:c.3050C>G	NP_059989.3:p.Ala1017Gly