Canonical Allele Identifier: CA366389094

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469983A>T (hg19) ; chr6:g.157148849A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148849A>T , CM000668.2:g.157148849A>T	GRCh38
NC_000006.11:g.157469983A>T , CM000668.1:g.157469983A>T	GRCh37
NC_000006.10:g.157511675A>T	NCBI36
NG_032093.1:g.375920A>T
NG_032093.2:g.375920A>T
NG_066624.1:g.377824A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2987A>T	ENSP00000055163.8:p.Gln996Leu
ENST00000414678.8:c.2897A>T	ENSP00000412835.3:p.Gln966Leu
ENST00000637015.2:c.2987A>T	ENSP00000489729.2:p.Gln996Leu
ENST00000319584.11:c.1001A>T	ENSP00000313006.7:p.Gln334Leu
ENST00000346085.10:c.3026A>T	ENSP00000344546.5:p.Gln1009Leu
ENST00000350026.10:c.2738A>T	ENSP00000055163.7:p.Gln913Leu
ENST00000414678.7:c.1145A>T	ENSP00000412835.2:p.Gln382Leu
ENST00000452544.2:n.888A>T
ENST00000635849.1:c.308A>T	ENSP00000490948.1:p.Gln103Leu
ENST00000636426.1:n.121A>T
ENST00000636930.2:c.2987A>T MANE Select	ENSP00000490491.2:p.Gln996Leu
ENST00000637015.1:c.226A>T
ENST00000637568.1:c.30A>T
ENST00000637810.1:c.488A>T	ENSP00000489636.1:p.Gln163Leu
ENST00000637904.1:c.488A>T	ENSP00000490550.1:p.Gln163Leu
ENST00000647938.1:c.2777A>T	ENSP00000498155.1:p.Gln926Leu
ENST00000674190.1:n.1736A>T
ENST00000319584.10:c.1004A>T	ENSP00000313006.6:p.Gln335Leu
ENST00000346085.9:c.2777A>T	ENSP00000344546.4:p.Gln926Leu
ENST00000350026.9:c.2738A>T	ENSP00000055163.7:p.Gln913Leu
ENST00000414678.6:c.1145A>T	ENSP00000412835.2:p.Gln382Leu
ENST00000452544.1:n.834A>T
ENST00000478761.3:c.60A>T
NM_017519.2:c.2738A>T	NP_059989.2:p.Gln913Leu
NM_020732.3:c.2777A>T	NP_065783.3:p.Gln926Leu
XM_005267069.3:c.2738A>T	XP_005267126.2:p.Gln913Leu
XM_011535984.1:c.1688A>T	XP_011534286.1:p.Gln563Leu
XM_011535985.1:c.1508A>T	XP_011534287.1:p.Gln503Leu
XM_011535986.1:c.1268A>T	XP_011534288.1:p.Gln423Leu
XM_011535987.1:c.887A>T	XP_011534289.1:p.Gln296Leu
XM_011535988.1:c.-20+15642A>T	XP_011534290.1:n.-20+15642A>T
NM_001346813.1:c.2738A>T	NP_001333742.1:p.Gln913Leu
NM_001363725.1:c.488A>T	NP_001350654.1:p.Gln163Leu
XM_011535984.2:c.2819A>T	XP_011534286.2:p.Gln940Leu
XM_011535988.3:c.-20+15642A>T	XP_011534290.1:n.-20+15642A>T
XM_017011103.2:c.2819A>T	XP_016866592.1:p.Gln940Leu
XM_017011104.1:c.2819A>T	XP_016866593.1:p.Gln940Leu
XM_017011105.2:c.2819A>T	XP_016866594.1:p.Gln940Leu
XM_017011106.2:c.2819A>T	XP_016866595.1:p.Gln940Leu
XM_017011107.2:c.2639A>T	XP_016866596.1:p.Gln880Leu
XR_002956289.1:n.2902A>T
NM_001363725.2:c.488A>T	NP_001350654.1:p.Gln163Leu
NM_001371656.1:c.3026A>T	NP_001358585.1:p.Gln1009Leu
NM_001374820.1:c.3026A>T	NP_001361749.1:p.Gln1009Leu
NM_001374828.1:c.2987A>T MANE Select	NP_001361757.1:p.Gln996Leu
NM_017519.3:c.2987A>T	NP_059989.3:p.Gln996Leu