Canonical Allele Identifier: CA366389298

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470080A>C (hg19) ; chr6:g.157148946A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148946A>C , CM000668.2:g.157148946A>C	GRCh38
NC_000006.11:g.157470080A>C , CM000668.1:g.157470080A>C	GRCh37
NC_000006.10:g.157511772A>C	NCBI36
NG_032093.1:g.376017A>C
NG_032093.2:g.376017A>C
NG_066624.1:g.377921A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3084A>C	ENSP00000055163.8:p.Gln1028His
ENST00000414678.8:c.2994A>C	ENSP00000412835.3:p.Gln998His
ENST00000637015.2:c.3084A>C	ENSP00000489729.2:p.Gln1028His
ENST00000319584.11:c.1098A>C	ENSP00000313006.7:p.Gln366His
ENST00000346085.10:c.3123A>C	ENSP00000344546.5:p.Gln1041His
ENST00000350026.10:c.2835A>C	ENSP00000055163.7:p.Gln945His
ENST00000414678.7:c.1242A>C	ENSP00000412835.2:p.Gln414His
ENST00000452544.2:n.985A>C
ENST00000635849.1:c.405A>C	ENSP00000490948.1:p.Gln135His
ENST00000635957.1:c.39A>C	ENSP00000490385.1:p.Gln13His
ENST00000636426.1:n.218A>C
ENST00000636930.2:c.3084A>C MANE Select	ENSP00000490491.2:p.Gln1028His
ENST00000637015.1:c.323A>C
ENST00000637568.1:c.127A>C
ENST00000637810.1:c.585A>C	ENSP00000489636.1:p.Gln195His
ENST00000637904.1:c.585A>C	ENSP00000490550.1:p.Gln195His
ENST00000647938.1:c.2874A>C	ENSP00000498155.1:p.Gln958His
ENST00000674190.1:n.1833A>C
ENST00000319584.10:c.1101A>C	ENSP00000313006.6:p.Gln367His
ENST00000346085.9:c.2874A>C	ENSP00000344546.4:p.Gln958His
ENST00000350026.9:c.2835A>C	ENSP00000055163.7:p.Gln945His
ENST00000400790.3:c.36A>C	ENSP00000383596.3:p.Gln12His
ENST00000414678.6:c.1242A>C	ENSP00000412835.2:p.Gln414His
ENST00000452544.1:n.931A>C
ENST00000478761.3:c.157A>C
NM_017519.2:c.2835A>C	NP_059989.2:p.Gln945His
NM_020732.3:c.2874A>C	NP_065783.3:p.Gln958His
XM_005267069.3:c.2835A>C	XP_005267126.2:p.Gln945His
XM_011535984.1:c.1785A>C	XP_011534286.1:p.Gln595His
XM_011535985.1:c.1605A>C	XP_011534287.1:p.Gln535His
XM_011535986.1:c.1365A>C	XP_011534288.1:p.Gln455His
XM_011535987.1:c.984A>C	XP_011534289.1:p.Gln328His
XM_011535988.1:c.-20+15739A>C	XP_011534290.1:n.-20+15739A>C
NM_001346813.1:c.2835A>C	NP_001333742.1:p.Gln945His
NM_001363725.1:c.585A>C	NP_001350654.1:p.Gln195His
XM_011535984.2:c.2916A>C	XP_011534286.2:p.Gln972His
XM_011535988.3:c.-20+15739A>C	XP_011534290.1:n.-20+15739A>C
XM_017011103.2:c.2916A>C	XP_016866592.1:p.Gln972His
XM_017011104.1:c.2916A>C	XP_016866593.1:p.Gln972His
XM_017011105.2:c.2916A>C	XP_016866594.1:p.Gln972His
XM_017011106.2:c.2916A>C	XP_016866595.1:p.Gln972His
XM_017011107.2:c.2736A>C	XP_016866596.1:p.Gln912His
XR_002956289.1:n.2999A>C
NM_001363725.2:c.585A>C	NP_001350654.1:p.Gln195His
NM_001371656.1:c.3123A>C	NP_001358585.1:p.Gln1041His
NM_001374820.1:c.3123A>C	NP_001361749.1:p.Gln1041His
NM_001374828.1:c.3084A>C MANE Select	NP_001361757.1:p.Gln1028His
NM_017519.3:c.3084A>C	NP_059989.3:p.Gln1028His