Canonical Allele Identifier: CA366389240

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470052T>C (hg19) ; chr6:g.157148918T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148918T>C , CM000668.2:g.157148918T>C	GRCh38
NC_000006.11:g.157470052T>C , CM000668.1:g.157470052T>C	GRCh37
NC_000006.10:g.157511744T>C	NCBI36
NG_032093.1:g.375989T>C
NG_032093.2:g.375989T>C
NG_066624.1:g.377893T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3056T>C	ENSP00000055163.8:p.Val1019Ala
ENST00000414678.8:c.2966T>C	ENSP00000412835.3:p.Val989Ala
ENST00000637015.2:c.3056T>C	ENSP00000489729.2:p.Val1019Ala
ENST00000319584.11:c.1070T>C	ENSP00000313006.7:p.Val357Ala
ENST00000346085.10:c.3095T>C	ENSP00000344546.5:p.Val1032Ala
ENST00000350026.10:c.2807T>C	ENSP00000055163.7:p.Val936Ala
ENST00000414678.7:c.1214T>C	ENSP00000412835.2:p.Val405Ala
ENST00000452544.2:n.957T>C
ENST00000635849.1:c.377T>C	ENSP00000490948.1:p.Val126Ala
ENST00000635957.1:c.11T>C	ENSP00000490385.1:p.Val4Ala
ENST00000636426.1:n.190T>C
ENST00000636930.2:c.3056T>C MANE Select	ENSP00000490491.2:p.Val1019Ala
ENST00000637015.1:c.295T>C
ENST00000637568.1:c.99T>C
ENST00000637810.1:c.557T>C	ENSP00000489636.1:p.Val186Ala
ENST00000637904.1:c.557T>C	ENSP00000490550.1:p.Val186Ala
ENST00000647938.1:c.2846T>C	ENSP00000498155.1:p.Val949Ala
ENST00000674190.1:n.1805T>C
ENST00000319584.10:c.1073T>C	ENSP00000313006.6:p.Val358Ala
ENST00000346085.9:c.2846T>C	ENSP00000344546.4:p.Val949Ala
ENST00000350026.9:c.2807T>C	ENSP00000055163.7:p.Val936Ala
ENST00000400790.3:c.8T>C	ENSP00000383596.3:p.Val3Ala
ENST00000414678.6:c.1214T>C	ENSP00000412835.2:p.Val405Ala
ENST00000452544.1:n.903T>C
ENST00000478761.3:c.129T>C
NM_017519.2:c.2807T>C	NP_059989.2:p.Val936Ala
NM_020732.3:c.2846T>C	NP_065783.3:p.Val949Ala
XM_005267069.3:c.2807T>C	XP_005267126.2:p.Val936Ala
XM_011535984.1:c.1757T>C	XP_011534286.1:p.Val586Ala
XM_011535985.1:c.1577T>C	XP_011534287.1:p.Val526Ala
XM_011535986.1:c.1337T>C	XP_011534288.1:p.Val446Ala
XM_011535987.1:c.956T>C	XP_011534289.1:p.Val319Ala
XM_011535988.1:c.-20+15711T>C	XP_011534290.1:n.-20+15711T>C
NM_001346813.1:c.2807T>C	NP_001333742.1:p.Val936Ala
NM_001363725.1:c.557T>C	NP_001350654.1:p.Val186Ala
XM_011535984.2:c.2888T>C	XP_011534286.2:p.Val963Ala
XM_011535988.3:c.-20+15711T>C	XP_011534290.1:n.-20+15711T>C
XM_017011103.2:c.2888T>C	XP_016866592.1:p.Val963Ala
XM_017011104.1:c.2888T>C	XP_016866593.1:p.Val963Ala
XM_017011105.2:c.2888T>C	XP_016866594.1:p.Val963Ala
XM_017011106.2:c.2888T>C	XP_016866595.1:p.Val963Ala
XM_017011107.2:c.2708T>C	XP_016866596.1:p.Val903Ala
XR_002956289.1:n.2971T>C
NM_001363725.2:c.557T>C	NP_001350654.1:p.Val186Ala
NM_001371656.1:c.3095T>C	NP_001358585.1:p.Val1032Ala
NM_001374820.1:c.3095T>C	NP_001361749.1:p.Val1032Ala
NM_001374828.1:c.3056T>C MANE Select	NP_001361757.1:p.Val1019Ala
NM_017519.3:c.3056T>C	NP_059989.3:p.Val1019Ala