Canonical Allele Identifier: CA366227809

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502207G>T (hg19) ; chr6:g.157181073G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181073G>T , CM000668.2:g.157181073G>T	GRCh38
NC_000006.11:g.157502207G>T , CM000668.1:g.157502207G>T	GRCh37
NC_000006.10:g.157543899G>T	NCBI36
NG_032093.1:g.408144G>T
NG_032093.2:g.408144G>T
NG_066624.1:g.410048G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3450G>T	ENSP00000055163.8:p.Met1150Ile
ENST00000414678.8:c.3519G>T	ENSP00000412835.3:p.Met1173Ile
ENST00000637015.2:c.3738G>T	ENSP00000489729.2:p.Met1246Ile
ENST00000319584.11:c.1623G>T	ENSP00000313006.7:p.Met541Ile
ENST00000346085.10:c.3489G>T	ENSP00000344546.5:p.Met1163Ile
ENST00000350026.10:c.3201G>T	ENSP00000055163.7:p.Met1067Ile
ENST00000414678.7:c.1767G>T	ENSP00000412835.2:p.Met589Ile
ENST00000635849.1:c.930G>T	ENSP00000490948.1:p.Met310Ile
ENST00000635957.1:c.564G>T	ENSP00000490385.1:p.Met188Ile
ENST00000636930.2:c.3609G>T MANE Select	ENSP00000490491.2:p.Met1203Ile
ENST00000636940.1:n.1606G>T
ENST00000637015.1:c.977G>T
ENST00000637568.1:c.891G>T
ENST00000637741.1:n.275G>T
ENST00000637810.1:c.951G>T	ENSP00000489636.1:p.Met317Ile
ENST00000637904.1:c.1110G>T	ENSP00000490550.1:p.Met370Ile
ENST00000647938.1:c.3240G>T	ENSP00000498155.1:p.Met1080Ile
ENST00000319584.10:c.1626G>T	ENSP00000313006.6:p.Met542Ile
ENST00000346085.9:c.3240G>T	ENSP00000344546.4:p.Met1080Ile
ENST00000350026.9:c.3201G>T	ENSP00000055163.7:p.Met1067Ile
ENST00000400790.3:c.402G>T	ENSP00000383596.3:p.Met134Ile
ENST00000414678.6:c.1767G>T	ENSP00000412835.2:p.Met589Ile
ENST00000478761.3:c.811G>T
NM_017519.2:c.3201G>T	NP_059989.2:p.Met1067Ile
NM_020732.3:c.3240G>T	NP_065783.3:p.Met1080Ile
XM_005267069.3:c.3360G>T	XP_005267126.2:p.Met1120Ile
XM_011535984.1:c.2439G>T	XP_011534286.1:p.Met813Ile
XM_011535985.1:c.2259G>T	XP_011534287.1:p.Met753Ile
XM_011535986.1:c.2019G>T	XP_011534288.1:p.Met673Ile
XM_011535987.1:c.1638G>T	XP_011534289.1:p.Met546Ile
XM_011535988.1:c.501G>T	XP_011534290.1:p.Met167Ile
NM_001346813.1:c.3360G>T	NP_001333742.1:p.Met1120Ile
NM_001363725.1:c.1110G>T	NP_001350654.1:p.Met370Ile
XM_011535984.2:c.3570G>T	XP_011534286.2:p.Met1190Ile
XM_011535988.3:c.501G>T	XP_011534290.1:p.Met167Ile
XM_017011103.2:c.3471G>T	XP_016866592.1:p.Met1157Ile
XM_017011104.1:c.3441G>T	XP_016866593.1:p.Met1147Ile
XM_017011105.2:c.3411G>T	XP_016866594.1:p.Met1137Ile
XM_017011106.2:c.3282G>T	XP_016866595.1:p.Met1094Ile
XM_017011107.2:c.3261G>T	XP_016866596.1:p.Met1087Ile
XR_002956289.1:n.3653G>T
NM_001363725.2:c.1110G>T	NP_001350654.1:p.Met370Ile
NM_001371656.1:c.3489G>T	NP_001358585.1:p.Met1163Ile
NM_001374820.1:c.3489G>T	NP_001361749.1:p.Met1163Ile
NM_001374828.1:c.3609G>T MANE Select	NP_001361757.1:p.Met1203Ile
NM_017519.3:c.3450G>T	NP_059989.3:p.Met1150Ile