Canonical Allele Identifier: CA366228140

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317510
• MyVariant Identifiers: chr6:g.157502252G>C (hg19) ; chr6:g.157181118G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181118G>C , CM000668.2:g.157181118G>C	GRCh38
NC_000006.11:g.157502252G>C , CM000668.1:g.157502252G>C	GRCh37
NC_000006.10:g.157543944G>C	NCBI36
NG_032093.1:g.408189G>C
NG_032093.2:g.408189G>C
NG_066624.1:g.410093G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3495G>C	ENSP00000055163.8:p.Lys1165Asn
ENST00000414678.8:c.3564G>C	ENSP00000412835.3:p.Lys1188Asn
ENST00000637015.2:c.3783G>C	ENSP00000489729.2:p.Lys1261Asn
ENST00000319584.11:c.1668G>C	ENSP00000313006.7:p.Lys556Asn
ENST00000346085.10:c.3534G>C	ENSP00000344546.5:p.Lys1178Asn
ENST00000350026.10:c.3246G>C	ENSP00000055163.7:p.Lys1082Asn
ENST00000414678.7:c.1812G>C	ENSP00000412835.2:p.Lys604Asn
ENST00000635849.1:c.975G>C	ENSP00000490948.1:p.Lys325Asn
ENST00000635957.1:c.609G>C	ENSP00000490385.1:p.Lys203Asn
ENST00000636930.2:c.3654G>C MANE Select	ENSP00000490491.2:p.Lys1218Asn
ENST00000636940.1:n.1651G>C
ENST00000637015.1:c.1022G>C
ENST00000637568.1:c.936G>C
ENST00000637741.1:n.320G>C
ENST00000637810.1:c.996G>C	ENSP00000489636.1:p.Lys332Asn
ENST00000637904.1:c.1155G>C	ENSP00000490550.1:p.Lys385Asn
ENST00000647938.1:c.3285G>C	ENSP00000498155.1:p.Lys1095Asn
ENST00000319584.10:c.1671G>C	ENSP00000313006.6:p.Lys557Asn
ENST00000346085.9:c.3285G>C	ENSP00000344546.4:p.Lys1095Asn
ENST00000350026.9:c.3246G>C	ENSP00000055163.7:p.Lys1082Asn
ENST00000400790.3:c.447G>C	ENSP00000383596.3:p.Lys149Asn
ENST00000414678.6:c.1812G>C	ENSP00000412835.2:p.Lys604Asn
ENST00000478761.3:c.856G>C
NM_017519.2:c.3246G>C	NP_059989.2:p.Lys1082Asn
NM_020732.3:c.3285G>C	NP_065783.3:p.Lys1095Asn
XM_005267069.3:c.3405G>C	XP_005267126.2:p.Lys1135Asn
XM_011535984.1:c.2484G>C	XP_011534286.1:p.Lys828Asn
XM_011535985.1:c.2304G>C	XP_011534287.1:p.Lys768Asn
XM_011535986.1:c.2064G>C	XP_011534288.1:p.Lys688Asn
XM_011535987.1:c.1683G>C	XP_011534289.1:p.Lys561Asn
XM_011535988.1:c.546G>C	XP_011534290.1:p.Lys182Asn
NM_001346813.1:c.3405G>C	NP_001333742.1:p.Lys1135Asn
NM_001363725.1:c.1155G>C	NP_001350654.1:p.Lys385Asn
XM_011535984.2:c.3615G>C	XP_011534286.2:p.Lys1205Asn
XM_011535988.3:c.546G>C	XP_011534290.1:p.Lys182Asn
XM_017011103.2:c.3516G>C	XP_016866592.1:p.Lys1172Asn
XM_017011104.1:c.3486G>C	XP_016866593.1:p.Lys1162Asn
XM_017011105.2:c.3456G>C	XP_016866594.1:p.Lys1152Asn
XM_017011106.2:c.3327G>C	XP_016866595.1:p.Lys1109Asn
XM_017011107.2:c.3306G>C	XP_016866596.1:p.Lys1102Asn
XR_002956289.1:n.3698G>C
NM_001363725.2:c.1155G>C	NP_001350654.1:p.Lys385Asn
NM_001371656.1:c.3534G>C	NP_001358585.1:p.Lys1178Asn
NM_001374820.1:c.3534G>C	NP_001361749.1:p.Lys1178Asn
NM_001374828.1:c.3654G>C MANE Select	NP_001361757.1:p.Lys1218Asn
NM_017519.3:c.3495G>C	NP_059989.3:p.Lys1165Asn