Canonical Allele Identifier: CA366389136

Gene: ARID1B

Linked Data

• dbSNP Id: rs1239914614
• MyVariant Identifiers: chr6:g.157470003C>T (hg19) ; chr6:g.157148869C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148869C>T , CM000668.2:g.157148869C>T	GRCh38
NC_000006.11:g.157470003C>T , CM000668.1:g.157470003C>T	GRCh37
NC_000006.10:g.157511695C>T	NCBI36
NG_032093.1:g.375940C>T
NG_032093.2:g.375940C>T
NG_066624.1:g.377844C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3007C>T	ENSP00000055163.8:p.Pro1003Ser
ENST00000414678.8:c.2917C>T	ENSP00000412835.3:p.Pro973Ser
ENST00000637015.2:c.3007C>T	ENSP00000489729.2:p.Pro1003Ser
ENST00000319584.11:c.1021C>T	ENSP00000313006.7:p.Pro341Ser
ENST00000346085.10:c.3046C>T	ENSP00000344546.5:p.Pro1016Ser
ENST00000350026.10:c.2758C>T	ENSP00000055163.7:p.Pro920Ser
ENST00000414678.7:c.1165C>T	ENSP00000412835.2:p.Pro389Ser
ENST00000452544.2:n.908C>T
ENST00000635849.1:c.328C>T	ENSP00000490948.1:p.Pro110Ser
ENST00000636426.1:n.141C>T
ENST00000636930.2:c.3007C>T MANE Select	ENSP00000490491.2:p.Pro1003Ser
ENST00000637015.1:c.246C>T
ENST00000637568.1:c.50C>T
ENST00000637810.1:c.508C>T	ENSP00000489636.1:p.Pro170Ser
ENST00000637904.1:c.508C>T	ENSP00000490550.1:p.Pro170Ser
ENST00000647938.1:c.2797C>T	ENSP00000498155.1:p.Pro933Ser
ENST00000674190.1:n.1756C>T
ENST00000319584.10:c.1024C>T	ENSP00000313006.6:p.Pro342Ser
ENST00000346085.9:c.2797C>T	ENSP00000344546.4:p.Pro933Ser
ENST00000350026.9:c.2758C>T	ENSP00000055163.7:p.Pro920Ser
ENST00000414678.6:c.1165C>T	ENSP00000412835.2:p.Pro389Ser
ENST00000452544.1:n.854C>T
ENST00000478761.3:c.80C>T
NM_017519.2:c.2758C>T	NP_059989.2:p.Pro920Ser
NM_020732.3:c.2797C>T	NP_065783.3:p.Pro933Ser
XM_005267069.3:c.2758C>T	XP_005267126.2:p.Pro920Ser
XM_011535984.1:c.1708C>T	XP_011534286.1:p.Pro570Ser
XM_011535985.1:c.1528C>T	XP_011534287.1:p.Pro510Ser
XM_011535986.1:c.1288C>T	XP_011534288.1:p.Pro430Ser
XM_011535987.1:c.907C>T	XP_011534289.1:p.Pro303Ser
XM_011535988.1:c.-20+15662C>T	XP_011534290.1:n.-20+15662C>T
NM_001346813.1:c.2758C>T	NP_001333742.1:p.Pro920Ser
NM_001363725.1:c.508C>T	NP_001350654.1:p.Pro170Ser
XM_011535984.2:c.2839C>T	XP_011534286.2:p.Pro947Ser
XM_011535988.3:c.-20+15662C>T	XP_011534290.1:n.-20+15662C>T
XM_017011103.2:c.2839C>T	XP_016866592.1:p.Pro947Ser
XM_017011104.1:c.2839C>T	XP_016866593.1:p.Pro947Ser
XM_017011105.2:c.2839C>T	XP_016866594.1:p.Pro947Ser
XM_017011106.2:c.2839C>T	XP_016866595.1:p.Pro947Ser
XM_017011107.2:c.2659C>T	XP_016866596.1:p.Pro887Ser
XR_002956289.1:n.2922C>T
NM_001363725.2:c.508C>T	NP_001350654.1:p.Pro170Ser
NM_001371656.1:c.3046C>T	NP_001358585.1:p.Pro1016Ser
NM_001374820.1:c.3046C>T	NP_001361749.1:p.Pro1016Ser
NM_001374828.1:c.3007C>T MANE Select	NP_001361757.1:p.Pro1003Ser
NM_017519.3:c.3007C>T	NP_059989.3:p.Pro1003Ser