Canonical Allele Identifier: CA366389150

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470011G>C (hg19) ; chr6:g.157148877G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148877G>C , CM000668.2:g.157148877G>C	GRCh38
NC_000006.11:g.157470011G>C , CM000668.1:g.157470011G>C	GRCh37
NC_000006.10:g.157511703G>C	NCBI36
NG_032093.1:g.375948G>C
NG_032093.2:g.375948G>C
NG_066624.1:g.377852G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3015G>C	ENSP00000055163.8:p.Met1005Ile
ENST00000414678.8:c.2925G>C	ENSP00000412835.3:p.Met975Ile
ENST00000637015.2:c.3015G>C	ENSP00000489729.2:p.Met1005Ile
ENST00000319584.11:c.1029G>C	ENSP00000313006.7:p.Met343Ile
ENST00000346085.10:c.3054G>C	ENSP00000344546.5:p.Met1018Ile
ENST00000350026.10:c.2766G>C	ENSP00000055163.7:p.Met922Ile
ENST00000414678.7:c.1173G>C	ENSP00000412835.2:p.Met391Ile
ENST00000452544.2:n.916G>C
ENST00000635849.1:c.336G>C	ENSP00000490948.1:p.Met112Ile
ENST00000636426.1:n.149G>C
ENST00000636930.2:c.3015G>C MANE Select	ENSP00000490491.2:p.Met1005Ile
ENST00000637015.1:c.254G>C
ENST00000637568.1:c.58G>C
ENST00000637810.1:c.516G>C	ENSP00000489636.1:p.Met172Ile
ENST00000637904.1:c.516G>C	ENSP00000490550.1:p.Met172Ile
ENST00000647938.1:c.2805G>C	ENSP00000498155.1:p.Met935Ile
ENST00000674190.1:n.1764G>C
ENST00000319584.10:c.1032G>C	ENSP00000313006.6:p.Met344Ile
ENST00000346085.9:c.2805G>C	ENSP00000344546.4:p.Met935Ile
ENST00000350026.9:c.2766G>C	ENSP00000055163.7:p.Met922Ile
ENST00000414678.6:c.1173G>C	ENSP00000412835.2:p.Met391Ile
ENST00000452544.1:n.862G>C
ENST00000478761.3:c.88G>C
NM_017519.2:c.2766G>C	NP_059989.2:p.Met922Ile
NM_020732.3:c.2805G>C	NP_065783.3:p.Met935Ile
XM_005267069.3:c.2766G>C	XP_005267126.2:p.Met922Ile
XM_011535984.1:c.1716G>C	XP_011534286.1:p.Met572Ile
XM_011535985.1:c.1536G>C	XP_011534287.1:p.Met512Ile
XM_011535986.1:c.1296G>C	XP_011534288.1:p.Met432Ile
XM_011535987.1:c.915G>C	XP_011534289.1:p.Met305Ile
XM_011535988.1:c.-20+15670G>C	XP_011534290.1:n.-20+15670G>C
NM_001346813.1:c.2766G>C	NP_001333742.1:p.Met922Ile
NM_001363725.1:c.516G>C	NP_001350654.1:p.Met172Ile
XM_011535984.2:c.2847G>C	XP_011534286.2:p.Met949Ile
XM_011535988.3:c.-20+15670G>C	XP_011534290.1:n.-20+15670G>C
XM_017011103.2:c.2847G>C	XP_016866592.1:p.Met949Ile
XM_017011104.1:c.2847G>C	XP_016866593.1:p.Met949Ile
XM_017011105.2:c.2847G>C	XP_016866594.1:p.Met949Ile
XM_017011106.2:c.2847G>C	XP_016866595.1:p.Met949Ile
XM_017011107.2:c.2667G>C	XP_016866596.1:p.Met889Ile
XR_002956289.1:n.2930G>C
NM_001363725.2:c.516G>C	NP_001350654.1:p.Met172Ile
NM_001371656.1:c.3054G>C	NP_001358585.1:p.Met1018Ile
NM_001374820.1:c.3054G>C	NP_001361749.1:p.Met1018Ile
NM_001374828.1:c.3015G>C MANE Select	NP_001361757.1:p.Met1005Ile
NM_017519.3:c.3015G>C	NP_059989.3:p.Met1005Ile