Canonical Allele Identifier: CA4067179

Gene: ARID1B

Linked Data

• dbSNP Id: rs374572368
• ExAC: 6:157470044 C / T
• gnomAD v2: 6-157470044-C-T
• gnomAD v3: 6-157148910-C-T
• gnomAD v4: 6-157148910-C-T
• MyVariant Identifiers: chr6:g.157470044C>T (hg19) ; chr6:g.157148910C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148910C>T , CM000668.2:g.157148910C>T	GRCh38
NC_000006.11:g.157470044C>T , CM000668.1:g.157470044C>T	GRCh37
NC_000006.10:g.157511736C>T	NCBI36
NG_032093.1:g.375981C>T
NG_032093.2:g.375981C>T
NG_066624.1:g.377885C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3048C>T	ENSP00000055163.8:p.Ala1016=
ENST00000414678.8:c.2958C>T	ENSP00000412835.3:p.Ala986=
ENST00000637015.2:c.3048C>T	ENSP00000489729.2:p.Ala1016=
ENST00000319584.11:c.1062C>T	ENSP00000313006.7:p.Ala354=
ENST00000346085.10:c.3087C>T	ENSP00000344546.5:p.Ala1029=
ENST00000350026.10:c.2799C>T	ENSP00000055163.7:p.Ala933=
ENST00000414678.7:c.1206C>T	ENSP00000412835.2:p.Ala402=
ENST00000452544.2:n.949C>T
ENST00000635849.1:c.369C>T	ENSP00000490948.1:p.Ala123=
ENST00000635957.1:c.3C>T	ENSP00000490385.1:p.Ala1=
ENST00000636426.1:n.182C>T
ENST00000636930.2:c.3048C>T MANE Select	ENSP00000490491.2:p.Ala1016=
ENST00000637015.1:c.287C>T
ENST00000637568.1:c.91C>T
ENST00000637810.1:c.549C>T	ENSP00000489636.1:p.Ala183=
ENST00000637904.1:c.549C>T	ENSP00000490550.1:p.Ala183=
ENST00000647938.1:c.2838C>T	ENSP00000498155.1:p.Ala946=
ENST00000674190.1:n.1797C>T
ENST00000319584.10:c.1065C>T	ENSP00000313006.6:p.Ala355=
ENST00000346085.9:c.2838C>T	ENSP00000344546.4:p.Ala946=
ENST00000350026.9:c.2799C>T	ENSP00000055163.7:p.Ala933=
ENST00000414678.6:c.1206C>T	ENSP00000412835.2:p.Ala402=
ENST00000452544.1:n.895C>T
ENST00000478761.3:c.121C>T
NM_017519.2:c.2799C>T	NP_059989.2:p.Ala933=
NM_020732.3:c.2838C>T	NP_065783.3:p.Ala946=
XM_005267069.3:c.2799C>T	XP_005267126.2:p.Ala933=
XM_011535984.1:c.1749C>T	XP_011534286.1:p.Ala583=
XM_011535985.1:c.1569C>T	XP_011534287.1:p.Ala523=
XM_011535986.1:c.1329C>T	XP_011534288.1:p.Ala443=
XM_011535987.1:c.948C>T	XP_011534289.1:p.Ala316=
XM_011535988.1:c.-20+15703C>T	XP_011534290.1:n.-20+15703C>T
NM_001346813.1:c.2799C>T	NP_001333742.1:p.Ala933=
NM_001363725.1:c.549C>T	NP_001350654.1:p.Ala183=
XM_011535984.2:c.2880C>T	XP_011534286.2:p.Ala960=
XM_011535988.3:c.-20+15703C>T	XP_011534290.1:n.-20+15703C>T
XM_017011103.2:c.2880C>T	XP_016866592.1:p.Ala960=
XM_017011104.1:c.2880C>T	XP_016866593.1:p.Ala960=
XM_017011105.2:c.2880C>T	XP_016866594.1:p.Ala960=
XM_017011106.2:c.2880C>T	XP_016866595.1:p.Ala960=
XM_017011107.2:c.2700C>T	XP_016866596.1:p.Ala900=
XR_002956289.1:n.2963C>T
NM_001363725.2:c.549C>T	NP_001350654.1:p.Ala183=
NM_001371656.1:c.3087C>T	NP_001358585.1:p.Ala1029=
NM_001374820.1:c.3087C>T	NP_001361749.1:p.Ala1029=
NM_001374828.1:c.3048C>T MANE Select	NP_001361757.1:p.Ala1016=
NM_017519.3:c.3048C>T	NP_059989.3:p.Ala1016=