Canonical Allele Identifier: CA366228106

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502245T>C (hg19) ; chr6:g.157181111T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181111T>C , CM000668.2:g.157181111T>C	GRCh38
NC_000006.11:g.157502245T>C , CM000668.1:g.157502245T>C	GRCh37
NC_000006.10:g.157543937T>C	NCBI36
NG_032093.1:g.408182T>C
NG_032093.2:g.408182T>C
NG_066624.1:g.410086T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3488T>C	ENSP00000055163.8:p.Val1163Ala
ENST00000414678.8:c.3557T>C	ENSP00000412835.3:p.Val1186Ala
ENST00000637015.2:c.3776T>C	ENSP00000489729.2:p.Val1259Ala
ENST00000319584.11:c.1661T>C	ENSP00000313006.7:p.Val554Ala
ENST00000346085.10:c.3527T>C	ENSP00000344546.5:p.Val1176Ala
ENST00000350026.10:c.3239T>C	ENSP00000055163.7:p.Val1080Ala
ENST00000414678.7:c.1805T>C	ENSP00000412835.2:p.Val602Ala
ENST00000635849.1:c.968T>C	ENSP00000490948.1:p.Val323Ala
ENST00000635957.1:c.602T>C	ENSP00000490385.1:p.Val201Ala
ENST00000636930.2:c.3647T>C MANE Select	ENSP00000490491.2:p.Val1216Ala
ENST00000636940.1:n.1644T>C
ENST00000637015.1:c.1015T>C
ENST00000637568.1:c.929T>C
ENST00000637741.1:n.313T>C
ENST00000637810.1:c.989T>C	ENSP00000489636.1:p.Val330Ala
ENST00000637904.1:c.1148T>C	ENSP00000490550.1:p.Val383Ala
ENST00000647938.1:c.3278T>C	ENSP00000498155.1:p.Val1093Ala
ENST00000319584.10:c.1664T>C	ENSP00000313006.6:p.Val555Ala
ENST00000346085.9:c.3278T>C	ENSP00000344546.4:p.Val1093Ala
ENST00000350026.9:c.3239T>C	ENSP00000055163.7:p.Val1080Ala
ENST00000400790.3:c.440T>C	ENSP00000383596.3:p.Val147Ala
ENST00000414678.6:c.1805T>C	ENSP00000412835.2:p.Val602Ala
ENST00000478761.3:c.849T>C
NM_017519.2:c.3239T>C	NP_059989.2:p.Val1080Ala
NM_020732.3:c.3278T>C	NP_065783.3:p.Val1093Ala
XM_005267069.3:c.3398T>C	XP_005267126.2:p.Val1133Ala
XM_011535984.1:c.2477T>C	XP_011534286.1:p.Val826Ala
XM_011535985.1:c.2297T>C	XP_011534287.1:p.Val766Ala
XM_011535986.1:c.2057T>C	XP_011534288.1:p.Val686Ala
XM_011535987.1:c.1676T>C	XP_011534289.1:p.Val559Ala
XM_011535988.1:c.539T>C	XP_011534290.1:p.Val180Ala
NM_001346813.1:c.3398T>C	NP_001333742.1:p.Val1133Ala
NM_001363725.1:c.1148T>C	NP_001350654.1:p.Val383Ala
XM_011535984.2:c.3608T>C	XP_011534286.2:p.Val1203Ala
XM_011535988.3:c.539T>C	XP_011534290.1:p.Val180Ala
XM_017011103.2:c.3509T>C	XP_016866592.1:p.Val1170Ala
XM_017011104.1:c.3479T>C	XP_016866593.1:p.Val1160Ala
XM_017011105.2:c.3449T>C	XP_016866594.1:p.Val1150Ala
XM_017011106.2:c.3320T>C	XP_016866595.1:p.Val1107Ala
XM_017011107.2:c.3299T>C	XP_016866596.1:p.Val1100Ala
XR_002956289.1:n.3691T>C
NM_001363725.2:c.1148T>C	NP_001350654.1:p.Val383Ala
NM_001371656.1:c.3527T>C	NP_001358585.1:p.Val1176Ala
NM_001374820.1:c.3527T>C	NP_001361749.1:p.Val1176Ala
NM_001374828.1:c.3647T>C MANE Select	NP_001361757.1:p.Val1216Ala
NM_017519.3:c.3488T>C	NP_059989.3:p.Val1163Ala