Canonical Allele Identifier: CA366242017

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374627
• MyVariant Identifiers: chr6:g.157522243G>C (hg19) ; chr6:g.157201109G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201109G>C , CM000668.2:g.157201109G>C	GRCh38
NC_000006.11:g.157522243G>C , CM000668.1:g.157522243G>C	GRCh37
NC_000006.10:g.157563935G>C	NCBI36
NG_032093.1:g.428180G>C
NG_032093.2:g.428180G>C
NG_066624.1:g.430084G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4725G>C	ENSP00000055163.8:p.Arg1575Ser
ENST00000414678.8:c.4794G>C	ENSP00000412835.3:p.Arg1598Ser
ENST00000637015.2:c.5013G>C	ENSP00000489729.2:p.Arg1671Ser
ENST00000346085.10:c.4764G>C	ENSP00000344546.5:p.Arg1588Ser
ENST00000350026.10:c.4476G>C	ENSP00000055163.7:p.Arg1492Ser
ENST00000414678.7:c.3042G>C	ENSP00000412835.2:p.Arg1014Ser
ENST00000635849.1:c.2205G>C	ENSP00000490948.1:p.Arg735Ser
ENST00000635957.1:c.1836G>C	ENSP00000490385.1:p.Arg612Ser
ENST00000636227.1:n.3347G>C
ENST00000636254.1:n.804G>C
ENST00000636930.2:c.4884G>C MANE Select	ENSP00000490491.2:p.Arg1628Ser
ENST00000636940.1:n.2881G>C
ENST00000637015.1:c.2252G>C
ENST00000637568.1:c.2166G>C
ENST00000637741.1:n.1550G>C
ENST00000637810.1:c.2226G>C	ENSP00000489636.1:p.Arg742Ser
ENST00000637904.1:c.2385G>C	ENSP00000490550.1:p.Arg795Ser
ENST00000647938.1:c.4515G>C	ENSP00000498155.1:p.Arg1505Ser
ENST00000346085.9:c.4515G>C	ENSP00000344546.4:p.Arg1505Ser
ENST00000350026.9:c.4476G>C	ENSP00000055163.7:p.Arg1492Ser
ENST00000414678.6:c.3042G>C	ENSP00000412835.2:p.Arg1014Ser
NM_017519.2:c.4476G>C	NP_059989.2:p.Arg1492Ser
NM_020732.3:c.4515G>C	NP_065783.3:p.Arg1505Ser
XM_005267069.3:c.4635G>C	XP_005267126.2:p.Arg1545Ser
XM_011535984.1:c.3714G>C	XP_011534286.1:p.Arg1238Ser
XM_011535985.1:c.3534G>C	XP_011534287.1:p.Arg1178Ser
XM_011535986.1:c.3294G>C	XP_011534288.1:p.Arg1098Ser
XM_011535987.1:c.2913G>C	XP_011534289.1:p.Arg971Ser
XM_011535988.1:c.1776G>C	XP_011534290.1:p.Arg592Ser
NM_001346813.1:c.4635G>C	NP_001333742.1:p.Arg1545Ser
NM_001363725.1:c.2385G>C	NP_001350654.1:p.Arg795Ser
XM_011535984.2:c.4845G>C	XP_011534286.2:p.Arg1615Ser
XM_011535988.3:c.1776G>C	XP_011534290.1:p.Arg592Ser
XM_017011103.2:c.4746G>C	XP_016866592.1:p.Arg1582Ser
XM_017011104.1:c.4716G>C	XP_016866593.1:p.Arg1572Ser
XM_017011105.2:c.4686G>C	XP_016866594.1:p.Arg1562Ser
XM_017011106.2:c.4557G>C	XP_016866595.1:p.Arg1519Ser
XM_017011107.2:c.4536G>C	XP_016866596.1:p.Arg1512Ser
XR_002956289.1:n.4831G>C
NM_001363725.2:c.2385G>C	NP_001350654.1:p.Arg795Ser
NM_001371656.1:c.4764G>C	NP_001358585.1:p.Arg1588Ser
NM_001374820.1:c.4764G>C	NP_001361749.1:p.Arg1588Ser
NM_001374828.1:c.4884G>C MANE Select	NP_001361757.1:p.Arg1628Ser
NM_017519.3:c.4725G>C	NP_059989.3:p.Arg1575Ser