Canonical Allele Identifier: CA366242485

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522448T>C (hg19) ; chr6:g.157201314T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201314T>C , CM000668.2:g.157201314T>C	GRCh38
NC_000006.11:g.157522448T>C , CM000668.1:g.157522448T>C	GRCh37
NC_000006.10:g.157564140T>C	NCBI36
NG_032093.1:g.428385T>C
NG_032093.2:g.428385T>C
NG_066624.1:g.430289T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4930T>C	ENSP00000055163.8:p.Phe1644Leu
ENST00000414678.8:c.4999T>C	ENSP00000412835.3:p.Phe1667Leu
ENST00000637015.2:c.5218T>C	ENSP00000489729.2:p.Phe1740Leu
ENST00000346085.10:c.4969T>C	ENSP00000344546.5:p.Phe1657Leu
ENST00000350026.10:c.4681T>C	ENSP00000055163.7:p.Phe1561Leu
ENST00000414678.7:c.3247T>C	ENSP00000412835.2:p.Phe1083Leu
ENST00000635849.1:c.2410T>C	ENSP00000490948.1:p.Phe804Leu
ENST00000635957.1:c.2041T>C	ENSP00000490385.1:p.Phe681Leu
ENST00000636227.1:n.3552T>C
ENST00000636254.1:n.1009T>C
ENST00000636930.2:c.5089T>C MANE Select	ENSP00000490491.2:p.Phe1697Leu
ENST00000636940.1:n.3086T>C
ENST00000637015.1:c.2457T>C
ENST00000637568.1:c.2371T>C
ENST00000637741.1:n.1755T>C
ENST00000637810.1:c.2431T>C	ENSP00000489636.1:p.Phe811Leu
ENST00000637904.1:c.2590T>C	ENSP00000490550.1:p.Phe864Leu
ENST00000647938.1:c.4720T>C	ENSP00000498155.1:p.Phe1574Leu
ENST00000346085.9:c.4720T>C	ENSP00000344546.4:p.Phe1574Leu
ENST00000350026.9:c.4681T>C	ENSP00000055163.7:p.Phe1561Leu
ENST00000414678.6:c.3247T>C	ENSP00000412835.2:p.Phe1083Leu
NM_017519.2:c.4681T>C	NP_059989.2:p.Phe1561Leu
NM_020732.3:c.4720T>C	NP_065783.3:p.Phe1574Leu
XM_005267069.3:c.4840T>C	XP_005267126.2:p.Phe1614Leu
XM_011535984.1:c.3919T>C	XP_011534286.1:p.Phe1307Leu
XM_011535985.1:c.3739T>C	XP_011534287.1:p.Phe1247Leu
XM_011535986.1:c.3499T>C	XP_011534288.1:p.Phe1167Leu
XM_011535987.1:c.3118T>C	XP_011534289.1:p.Phe1040Leu
XM_011535988.1:c.1981T>C	XP_011534290.1:p.Phe661Leu
NM_001346813.1:c.4840T>C	NP_001333742.1:p.Phe1614Leu
NM_001363725.1:c.2590T>C	NP_001350654.1:p.Phe864Leu
XM_011535984.2:c.5050T>C	XP_011534286.2:p.Phe1684Leu
XM_011535988.3:c.1981T>C	XP_011534290.1:p.Phe661Leu
XM_017011103.2:c.4951T>C	XP_016866592.1:p.Phe1651Leu
XM_017011104.1:c.4921T>C	XP_016866593.1:p.Phe1641Leu
XM_017011105.2:c.4891T>C	XP_016866594.1:p.Phe1631Leu
XM_017011106.2:c.4762T>C	XP_016866595.1:p.Phe1588Leu
XM_017011107.2:c.4741T>C	XP_016866596.1:p.Phe1581Leu
XR_002956289.1:n.5036T>C
NM_001363725.2:c.2590T>C	NP_001350654.1:p.Phe864Leu
NM_001371656.1:c.4969T>C	NP_001358585.1:p.Phe1657Leu
NM_001374820.1:c.4969T>C	NP_001361749.1:p.Phe1657Leu
NM_001374828.1:c.5089T>C MANE Select	NP_001361757.1:p.Phe1697Leu
NM_017519.3:c.4930T>C	NP_059989.3:p.Phe1644Leu