Canonical Allele Identifier: CA366389228

Gene: ARID1B

Linked Data

• COSMIC: COSM3948314 ; COSM3948315
• MyVariant Identifiers: chr6:g.157470046C>T (hg19) ; chr6:g.157148912C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148912C>T , CM000668.2:g.157148912C>T	GRCh38
NC_000006.11:g.157470046C>T , CM000668.1:g.157470046C>T	GRCh37
NC_000006.10:g.157511738C>T	NCBI36
NG_032093.1:g.375983C>T
NG_032093.2:g.375983C>T
NG_066624.1:g.377887C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3050C>T	ENSP00000055163.8:p.Ala1017Val
ENST00000414678.8:c.2960C>T	ENSP00000412835.3:p.Ala987Val
ENST00000637015.2:c.3050C>T	ENSP00000489729.2:p.Ala1017Val
ENST00000319584.11:c.1064C>T	ENSP00000313006.7:p.Ala355Val
ENST00000346085.10:c.3089C>T	ENSP00000344546.5:p.Ala1030Val
ENST00000350026.10:c.2801C>T	ENSP00000055163.7:p.Ala934Val
ENST00000414678.7:c.1208C>T	ENSP00000412835.2:p.Ala403Val
ENST00000452544.2:n.951C>T
ENST00000635849.1:c.371C>T	ENSP00000490948.1:p.Ala124Val
ENST00000635957.1:c.5C>T	ENSP00000490385.1:p.Ala2Val
ENST00000636426.1:n.184C>T
ENST00000636930.2:c.3050C>T MANE Select	ENSP00000490491.2:p.Ala1017Val
ENST00000637015.1:c.289C>T
ENST00000637568.1:c.93C>T
ENST00000637810.1:c.551C>T	ENSP00000489636.1:p.Ala184Val
ENST00000637904.1:c.551C>T	ENSP00000490550.1:p.Ala184Val
ENST00000647938.1:c.2840C>T	ENSP00000498155.1:p.Ala947Val
ENST00000674190.1:n.1799C>T
ENST00000319584.10:c.1067C>T	ENSP00000313006.6:p.Ala356Val
ENST00000346085.9:c.2840C>T	ENSP00000344546.4:p.Ala947Val
ENST00000350026.9:c.2801C>T	ENSP00000055163.7:p.Ala934Val
ENST00000400790.3:c.2C>T	ENSP00000383596.3:p.Ala1Val
ENST00000414678.6:c.1208C>T	ENSP00000412835.2:p.Ala403Val
ENST00000452544.1:n.897C>T
ENST00000478761.3:c.123C>T
NM_017519.2:c.2801C>T	NP_059989.2:p.Ala934Val
NM_020732.3:c.2840C>T	NP_065783.3:p.Ala947Val
XM_005267069.3:c.2801C>T	XP_005267126.2:p.Ala934Val
XM_011535984.1:c.1751C>T	XP_011534286.1:p.Ala584Val
XM_011535985.1:c.1571C>T	XP_011534287.1:p.Ala524Val
XM_011535986.1:c.1331C>T	XP_011534288.1:p.Ala444Val
XM_011535987.1:c.950C>T	XP_011534289.1:p.Ala317Val
XM_011535988.1:c.-20+15705C>T	XP_011534290.1:n.-20+15705C>T
NM_001346813.1:c.2801C>T	NP_001333742.1:p.Ala934Val
NM_001363725.1:c.551C>T	NP_001350654.1:p.Ala184Val
XM_011535984.2:c.2882C>T	XP_011534286.2:p.Ala961Val
XM_011535988.3:c.-20+15705C>T	XP_011534290.1:n.-20+15705C>T
XM_017011103.2:c.2882C>T	XP_016866592.1:p.Ala961Val
XM_017011104.1:c.2882C>T	XP_016866593.1:p.Ala961Val
XM_017011105.2:c.2882C>T	XP_016866594.1:p.Ala961Val
XM_017011106.2:c.2882C>T	XP_016866595.1:p.Ala961Val
XM_017011107.2:c.2702C>T	XP_016866596.1:p.Ala901Val
XR_002956289.1:n.2965C>T
NM_001363725.2:c.551C>T	NP_001350654.1:p.Ala184Val
NM_001371656.1:c.3089C>T	NP_001358585.1:p.Ala1030Val
NM_001374820.1:c.3089C>T	NP_001361749.1:p.Ala1030Val
NM_001374828.1:c.3050C>T MANE Select	NP_001361757.1:p.Ala1017Val
NM_017519.3:c.3050C>T	NP_059989.3:p.Ala1017Val