Canonical Allele Identifier: CA366228376

Gene: ARID1B

Linked Data

• dbSNP Id: rs1282312643
• MyVariant Identifiers: chr6:g.157502286G>C (hg19) ; chr6:g.157181152G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181152G>C , CM000668.2:g.157181152G>C	GRCh38
NC_000006.11:g.157502286G>C , CM000668.1:g.157502286G>C	GRCh37
NC_000006.10:g.157543978G>C	NCBI36
NG_032093.1:g.408223G>C
NG_032093.2:g.408223G>C
NG_066624.1:g.410127G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3529G>C	ENSP00000055163.8:p.Val1177Leu
ENST00000414678.8:c.3598G>C	ENSP00000412835.3:p.Val1200Leu
ENST00000637015.2:c.3817G>C	ENSP00000489729.2:p.Val1273Leu
ENST00000319584.11:c.1702G>C	ENSP00000313006.7:p.Val568Leu
ENST00000346085.10:c.3568G>C	ENSP00000344546.5:p.Val1190Leu
ENST00000350026.10:c.3280G>C	ENSP00000055163.7:p.Val1094Leu
ENST00000414678.7:c.1846G>C	ENSP00000412835.2:p.Val616Leu
ENST00000635849.1:c.1009G>C	ENSP00000490948.1:p.Val337Leu
ENST00000635957.1:c.643G>C	ENSP00000490385.1:p.Val215Leu
ENST00000636930.2:c.3688G>C MANE Select	ENSP00000490491.2:p.Val1230Leu
ENST00000636940.1:n.1685G>C
ENST00000637015.1:c.1056G>C
ENST00000637568.1:c.970G>C
ENST00000637741.1:n.354G>C
ENST00000637810.1:c.1030G>C	ENSP00000489636.1:p.Val344Leu
ENST00000637904.1:c.1189G>C	ENSP00000490550.1:p.Val397Leu
ENST00000647938.1:c.3319G>C	ENSP00000498155.1:p.Val1107Leu
ENST00000319584.10:c.1705G>C	ENSP00000313006.6:p.Val569Leu
ENST00000346085.9:c.3319G>C	ENSP00000344546.4:p.Val1107Leu
ENST00000350026.9:c.3280G>C	ENSP00000055163.7:p.Val1094Leu
ENST00000400790.3:c.481G>C	ENSP00000383596.3:p.Val161Leu
ENST00000414678.6:c.1846G>C	ENSP00000412835.2:p.Val616Leu
ENST00000478761.3:c.890G>C
NM_017519.2:c.3280G>C	NP_059989.2:p.Val1094Leu
NM_020732.3:c.3319G>C	NP_065783.3:p.Val1107Leu
XM_005267069.3:c.3439G>C	XP_005267126.2:p.Val1147Leu
XM_011535984.1:c.2518G>C	XP_011534286.1:p.Val840Leu
XM_011535985.1:c.2338G>C	XP_011534287.1:p.Val780Leu
XM_011535986.1:c.2098G>C	XP_011534288.1:p.Val700Leu
XM_011535987.1:c.1717G>C	XP_011534289.1:p.Val573Leu
XM_011535988.1:c.580G>C	XP_011534290.1:p.Val194Leu
NM_001346813.1:c.3439G>C	NP_001333742.1:p.Val1147Leu
NM_001363725.1:c.1189G>C	NP_001350654.1:p.Val397Leu
XM_011535984.2:c.3649G>C	XP_011534286.2:p.Val1217Leu
XM_011535988.3:c.580G>C	XP_011534290.1:p.Val194Leu
XM_017011103.2:c.3550G>C	XP_016866592.1:p.Val1184Leu
XM_017011104.1:c.3520G>C	XP_016866593.1:p.Val1174Leu
XM_017011105.2:c.3490G>C	XP_016866594.1:p.Val1164Leu
XM_017011106.2:c.3361G>C	XP_016866595.1:p.Val1121Leu
XM_017011107.2:c.3340G>C	XP_016866596.1:p.Val1114Leu
XR_002956289.1:n.3732G>C
NM_001363725.2:c.1189G>C	NP_001350654.1:p.Val397Leu
NM_001371656.1:c.3568G>C	NP_001358585.1:p.Val1190Leu
NM_001374820.1:c.3568G>C	NP_001361749.1:p.Val1190Leu
NM_001374828.1:c.3688G>C MANE Select	NP_001361757.1:p.Val1230Leu
NM_017519.3:c.3529G>C	NP_059989.3:p.Val1177Leu