Canonical Allele Identifier: CA366234339

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510902T>A (hg19) ; chr6:g.157189768T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189768T>A , CM000668.2:g.157189768T>A	GRCh38
NC_000006.11:g.157510902T>A , CM000668.1:g.157510902T>A	GRCh37
NC_000006.10:g.157552594T>A	NCBI36
NG_032093.1:g.416839T>A
NG_032093.2:g.416839T>A
NG_066624.1:g.418743T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3887T>A	ENSP00000055163.8:p.Met1296Lys
ENST00000414678.8:c.3956T>A	ENSP00000412835.3:p.Met1319Lys
ENST00000637015.2:c.4175T>A	ENSP00000489729.2:p.Met1392Lys
ENST00000346085.10:c.3926T>A	ENSP00000344546.5:p.Met1309Lys
ENST00000350026.10:c.3638T>A	ENSP00000055163.7:p.Met1213Lys
ENST00000414678.7:c.2204T>A	ENSP00000412835.2:p.Met735Lys
ENST00000635849.1:c.1367T>A	ENSP00000490948.1:p.Met456Lys
ENST00000635957.1:c.1001T>A	ENSP00000490385.1:p.Met334Lys
ENST00000636930.2:c.4046T>A MANE Select	ENSP00000490491.2:p.Met1349Lys
ENST00000636940.1:n.2043T>A
ENST00000637015.1:c.1414T>A
ENST00000637568.1:c.1328T>A
ENST00000637741.1:n.712T>A
ENST00000637810.1:c.1388T>A	ENSP00000489636.1:p.Met463Lys
ENST00000637904.1:c.1547T>A	ENSP00000490550.1:p.Met516Lys
ENST00000647938.1:c.3677T>A	ENSP00000498155.1:p.Met1226Lys
ENST00000346085.9:c.3677T>A	ENSP00000344546.4:p.Met1226Lys
ENST00000350026.9:c.3638T>A	ENSP00000055163.7:p.Met1213Lys
ENST00000414678.6:c.2204T>A	ENSP00000412835.2:p.Met735Lys
NM_017519.2:c.3638T>A	NP_059989.2:p.Met1213Lys
NM_020732.3:c.3677T>A	NP_065783.3:p.Met1226Lys
XM_005267069.3:c.3797T>A	XP_005267126.2:p.Met1266Lys
XM_011535984.1:c.2876T>A	XP_011534286.1:p.Met959Lys
XM_011535985.1:c.2696T>A	XP_011534287.1:p.Met899Lys
XM_011535986.1:c.2456T>A	XP_011534288.1:p.Met819Lys
XM_011535987.1:c.2075T>A	XP_011534289.1:p.Met692Lys
XM_011535988.1:c.938T>A	XP_011534290.1:p.Met313Lys
NM_001346813.1:c.3797T>A	NP_001333742.1:p.Met1266Lys
NM_001363725.1:c.1547T>A	NP_001350654.1:p.Met516Lys
XM_011535984.2:c.4007T>A	XP_011534286.2:p.Met1336Lys
XM_011535988.3:c.938T>A	XP_011534290.1:p.Met313Lys
XM_017011103.2:c.3908T>A	XP_016866592.1:p.Met1303Lys
XM_017011104.1:c.3878T>A	XP_016866593.1:p.Met1293Lys
XM_017011105.2:c.3848T>A	XP_016866594.1:p.Met1283Lys
XM_017011106.2:c.3719T>A	XP_016866595.1:p.Met1240Lys
XM_017011107.2:c.3698T>A	XP_016866596.1:p.Met1233Lys
XR_002956289.1:n.4090T>A
NM_001363725.2:c.1547T>A	NP_001350654.1:p.Met516Lys
NM_001371656.1:c.3926T>A	NP_001358585.1:p.Met1309Lys
NM_001374820.1:c.3926T>A	NP_001361749.1:p.Met1309Lys
NM_001374828.1:c.4046T>A MANE Select	NP_001361757.1:p.Met1349Lys
NM_017519.3:c.3887T>A	NP_059989.3:p.Met1296Lys