Canonical Allele Identifier: CA366389010

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128634554
• MyVariant Identifiers: chr6:g.157469947G>A (hg19) ; chr6:g.157148813G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148813G>A , CM000668.2:g.157148813G>A	GRCh38
NC_000006.11:g.157469947G>A , CM000668.1:g.157469947G>A	GRCh37
NC_000006.10:g.157511639G>A	NCBI36
NG_032093.1:g.375884G>A
NG_032093.2:g.375884G>A
NG_066624.1:g.377788G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2951G>A	ENSP00000055163.8:p.Ser984Asn
ENST00000414678.8:c.2861G>A	ENSP00000412835.3:p.Ser954Asn
ENST00000637015.2:c.2951G>A	ENSP00000489729.2:p.Ser984Asn
ENST00000319584.11:c.965G>A	ENSP00000313006.7:p.Ser322Asn
ENST00000346085.10:c.2990G>A	ENSP00000344546.5:p.Ser997Asn
ENST00000350026.10:c.2702G>A	ENSP00000055163.7:p.Ser901Asn
ENST00000414678.7:c.1109G>A	ENSP00000412835.2:p.Ser370Asn
ENST00000452544.2:n.852G>A
ENST00000635849.1:c.272G>A	ENSP00000490948.1:p.Ser91Asn
ENST00000636426.1:n.85G>A
ENST00000636930.2:c.2951G>A MANE Select	ENSP00000490491.2:p.Ser984Asn
ENST00000637015.1:c.190G>A
ENST00000637810.1:c.452G>A	ENSP00000489636.1:p.Ser151Asn
ENST00000637904.1:c.452G>A	ENSP00000490550.1:p.Ser151Asn
ENST00000647938.1:c.2741G>A	ENSP00000498155.1:p.Ser914Asn
ENST00000674190.1:n.1700G>A
ENST00000319584.10:c.968G>A	ENSP00000313006.6:p.Ser323Asn
ENST00000346085.9:c.2741G>A	ENSP00000344546.4:p.Ser914Asn
ENST00000350026.9:c.2702G>A	ENSP00000055163.7:p.Ser901Asn
ENST00000414678.6:c.1109G>A	ENSP00000412835.2:p.Ser370Asn
ENST00000452544.1:n.798G>A
ENST00000478761.3:c.24G>A
NM_017519.2:c.2702G>A	NP_059989.2:p.Ser901Asn
NM_020732.3:c.2741G>A	NP_065783.3:p.Ser914Asn
XM_005267069.3:c.2702G>A	XP_005267126.2:p.Ser901Asn
XM_011535984.1:c.1652G>A	XP_011534286.1:p.Ser551Asn
XM_011535985.1:c.1472G>A	XP_011534287.1:p.Ser491Asn
XM_011535986.1:c.1232G>A	XP_011534288.1:p.Ser411Asn
XM_011535987.1:c.851G>A	XP_011534289.1:p.Ser284Asn
XM_011535988.1:c.-20+15606G>A	XP_011534290.1:n.-20+15606G>A
NM_001346813.1:c.2702G>A	NP_001333742.1:p.Ser901Asn
NM_001363725.1:c.452G>A	NP_001350654.1:p.Ser151Asn
XM_011535984.2:c.2783G>A	XP_011534286.2:p.Ser928Asn
XM_011535988.3:c.-20+15606G>A	XP_011534290.1:n.-20+15606G>A
XM_017011103.2:c.2783G>A	XP_016866592.1:p.Ser928Asn
XM_017011104.1:c.2783G>A	XP_016866593.1:p.Ser928Asn
XM_017011105.2:c.2783G>A	XP_016866594.1:p.Ser928Asn
XM_017011106.2:c.2783G>A	XP_016866595.1:p.Ser928Asn
XM_017011107.2:c.2603G>A	XP_016866596.1:p.Ser868Asn
XR_002956289.1:n.2866G>A
NM_001363725.2:c.452G>A	NP_001350654.1:p.Ser151Asn
NM_001371656.1:c.2990G>A	NP_001358585.1:p.Ser997Asn
NM_001374820.1:c.2990G>A	NP_001361749.1:p.Ser997Asn
NM_001374828.1:c.2951G>A MANE Select	NP_001361757.1:p.Ser984Asn
NM_017519.3:c.2951G>A	NP_059989.3:p.Ser984Asn