Canonical Allele Identifier: CA366242508

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522452T>C (hg19) ; chr6:g.157201318T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201318T>C , CM000668.2:g.157201318T>C	GRCh38
NC_000006.11:g.157522452T>C , CM000668.1:g.157522452T>C	GRCh37
NC_000006.10:g.157564144T>C	NCBI36
NG_032093.1:g.428389T>C
NG_032093.2:g.428389T>C
NG_066624.1:g.430293T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4934T>C	ENSP00000055163.8:p.Leu1645Pro
ENST00000414678.8:c.5003T>C	ENSP00000412835.3:p.Leu1668Pro
ENST00000637015.2:c.5222T>C	ENSP00000489729.2:p.Leu1741Pro
ENST00000346085.10:c.4973T>C	ENSP00000344546.5:p.Leu1658Pro
ENST00000350026.10:c.4685T>C	ENSP00000055163.7:p.Leu1562Pro
ENST00000414678.7:c.3251T>C	ENSP00000412835.2:p.Leu1084Pro
ENST00000635849.1:c.2414T>C	ENSP00000490948.1:p.Leu805Pro
ENST00000635957.1:c.2045T>C	ENSP00000490385.1:p.Leu682Pro
ENST00000636227.1:n.3556T>C
ENST00000636254.1:n.1013T>C
ENST00000636930.2:c.5093T>C MANE Select	ENSP00000490491.2:p.Leu1698Pro
ENST00000636940.1:n.3090T>C
ENST00000637015.1:c.2461T>C
ENST00000637568.1:c.2375T>C
ENST00000637741.1:n.1759T>C
ENST00000637810.1:c.2435T>C	ENSP00000489636.1:p.Leu812Pro
ENST00000637904.1:c.2594T>C	ENSP00000490550.1:p.Leu865Pro
ENST00000647938.1:c.4724T>C	ENSP00000498155.1:p.Leu1575Pro
ENST00000346085.9:c.4724T>C	ENSP00000344546.4:p.Leu1575Pro
ENST00000350026.9:c.4685T>C	ENSP00000055163.7:p.Leu1562Pro
ENST00000414678.6:c.3251T>C	ENSP00000412835.2:p.Leu1084Pro
NM_017519.2:c.4685T>C	NP_059989.2:p.Leu1562Pro
NM_020732.3:c.4724T>C	NP_065783.3:p.Leu1575Pro
XM_005267069.3:c.4844T>C	XP_005267126.2:p.Leu1615Pro
XM_011535984.1:c.3923T>C	XP_011534286.1:p.Leu1308Pro
XM_011535985.1:c.3743T>C	XP_011534287.1:p.Leu1248Pro
XM_011535986.1:c.3503T>C	XP_011534288.1:p.Leu1168Pro
XM_011535987.1:c.3122T>C	XP_011534289.1:p.Leu1041Pro
XM_011535988.1:c.1985T>C	XP_011534290.1:p.Leu662Pro
NM_001346813.1:c.4844T>C	NP_001333742.1:p.Leu1615Pro
NM_001363725.1:c.2594T>C	NP_001350654.1:p.Leu865Pro
XM_011535984.2:c.5054T>C	XP_011534286.2:p.Leu1685Pro
XM_011535988.3:c.1985T>C	XP_011534290.1:p.Leu662Pro
XM_017011103.2:c.4955T>C	XP_016866592.1:p.Leu1652Pro
XM_017011104.1:c.4925T>C	XP_016866593.1:p.Leu1642Pro
XM_017011105.2:c.4895T>C	XP_016866594.1:p.Leu1632Pro
XM_017011106.2:c.4766T>C	XP_016866595.1:p.Leu1589Pro
XM_017011107.2:c.4745T>C	XP_016866596.1:p.Leu1582Pro
XR_002956289.1:n.5040T>C
NM_001363725.2:c.2594T>C	NP_001350654.1:p.Leu865Pro
NM_001371656.1:c.4973T>C	NP_001358585.1:p.Leu1658Pro
NM_001374820.1:c.4973T>C	NP_001361749.1:p.Leu1658Pro
NM_001374828.1:c.5093T>C MANE Select	NP_001361757.1:p.Leu1698Pro
NM_017519.3:c.4934T>C	NP_059989.3:p.Leu1645Pro