Canonical Allele Identifier: CA366389155

Gene: ARID1B

Linked Data

• dbSNP Id: rs1789994428
• gnomAD v4: 6-157148878-C-T
• MyVariant Identifiers: chr6:g.157470012C>T (hg19) ; chr6:g.157148878C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148878C>T , CM000668.2:g.157148878C>T	GRCh38
NC_000006.11:g.157470012C>T , CM000668.1:g.157470012C>T	GRCh37
NC_000006.10:g.157511704C>T	NCBI36
NG_032093.1:g.375949C>T
NG_032093.2:g.375949C>T
NG_066624.1:g.377853C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3016C>T	ENSP00000055163.8:p.Pro1006Ser
ENST00000414678.8:c.2926C>T	ENSP00000412835.3:p.Pro976Ser
ENST00000637015.2:c.3016C>T	ENSP00000489729.2:p.Pro1006Ser
ENST00000319584.11:c.1030C>T	ENSP00000313006.7:p.Pro344Ser
ENST00000346085.10:c.3055C>T	ENSP00000344546.5:p.Pro1019Ser
ENST00000350026.10:c.2767C>T	ENSP00000055163.7:p.Pro923Ser
ENST00000414678.7:c.1174C>T	ENSP00000412835.2:p.Pro392Ser
ENST00000452544.2:n.917C>T
ENST00000635849.1:c.337C>T	ENSP00000490948.1:p.Pro113Ser
ENST00000636426.1:n.150C>T
ENST00000636930.2:c.3016C>T MANE Select	ENSP00000490491.2:p.Pro1006Ser
ENST00000637015.1:c.255C>T
ENST00000637568.1:c.59C>T
ENST00000637810.1:c.517C>T	ENSP00000489636.1:p.Pro173Ser
ENST00000637904.1:c.517C>T	ENSP00000490550.1:p.Pro173Ser
ENST00000647938.1:c.2806C>T	ENSP00000498155.1:p.Pro936Ser
ENST00000674190.1:n.1765C>T
ENST00000319584.10:c.1033C>T	ENSP00000313006.6:p.Pro345Ser
ENST00000346085.9:c.2806C>T	ENSP00000344546.4:p.Pro936Ser
ENST00000350026.9:c.2767C>T	ENSP00000055163.7:p.Pro923Ser
ENST00000414678.6:c.1174C>T	ENSP00000412835.2:p.Pro392Ser
ENST00000452544.1:n.863C>T
ENST00000478761.3:c.89C>T
NM_017519.2:c.2767C>T	NP_059989.2:p.Pro923Ser
NM_020732.3:c.2806C>T	NP_065783.3:p.Pro936Ser
XM_005267069.3:c.2767C>T	XP_005267126.2:p.Pro923Ser
XM_011535984.1:c.1717C>T	XP_011534286.1:p.Pro573Ser
XM_011535985.1:c.1537C>T	XP_011534287.1:p.Pro513Ser
XM_011535986.1:c.1297C>T	XP_011534288.1:p.Pro433Ser
XM_011535987.1:c.916C>T	XP_011534289.1:p.Pro306Ser
XM_011535988.1:c.-20+15671C>T	XP_011534290.1:n.-20+15671C>T
NM_001346813.1:c.2767C>T	NP_001333742.1:p.Pro923Ser
NM_001363725.1:c.517C>T	NP_001350654.1:p.Pro173Ser
XM_011535984.2:c.2848C>T	XP_011534286.2:p.Pro950Ser
XM_011535988.3:c.-20+15671C>T	XP_011534290.1:n.-20+15671C>T
XM_017011103.2:c.2848C>T	XP_016866592.1:p.Pro950Ser
XM_017011104.1:c.2848C>T	XP_016866593.1:p.Pro950Ser
XM_017011105.2:c.2848C>T	XP_016866594.1:p.Pro950Ser
XM_017011106.2:c.2848C>T	XP_016866595.1:p.Pro950Ser
XM_017011107.2:c.2668C>T	XP_016866596.1:p.Pro890Ser
XR_002956289.1:n.2931C>T
NM_001363725.2:c.517C>T	NP_001350654.1:p.Pro173Ser
NM_001371656.1:c.3055C>T	NP_001358585.1:p.Pro1019Ser
NM_001374820.1:c.3055C>T	NP_001361749.1:p.Pro1019Ser
NM_001374828.1:c.3016C>T MANE Select	NP_001361757.1:p.Pro1006Ser
NM_017519.3:c.3016C>T	NP_059989.3:p.Pro1006Ser