Canonical Allele Identifier: CA366388955

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469923A>C (hg19) ; chr6:g.157148789A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148789A>C , CM000668.2:g.157148789A>C	GRCh38
NC_000006.11:g.157469923A>C , CM000668.1:g.157469923A>C	GRCh37
NC_000006.10:g.157511615A>C	NCBI36
NG_032093.1:g.375860A>C
NG_032093.2:g.375860A>C
NG_066624.1:g.377764A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2927A>C	ENSP00000055163.8:p.Asn976Thr
ENST00000414678.8:c.2837A>C	ENSP00000412835.3:p.Asn946Thr
ENST00000637015.2:c.2927A>C	ENSP00000489729.2:p.Asn976Thr
ENST00000319584.11:c.941A>C	ENSP00000313006.7:p.Asn314Thr
ENST00000346085.10:c.2966A>C	ENSP00000344546.5:p.Asn989Thr
ENST00000350026.10:c.2678A>C	ENSP00000055163.7:p.Asn893Thr
ENST00000414678.7:c.1085A>C	ENSP00000412835.2:p.Asn362Thr
ENST00000452544.2:n.828A>C
ENST00000635849.1:c.248A>C	ENSP00000490948.1:p.Asn83Thr
ENST00000636426.1:n.61A>C
ENST00000636930.2:c.2927A>C MANE Select	ENSP00000490491.2:p.Asn976Thr
ENST00000637015.1:c.166A>C
ENST00000637810.1:c.428A>C	ENSP00000489636.1:p.Asn143Thr
ENST00000637904.1:c.428A>C	ENSP00000490550.1:p.Asn143Thr
ENST00000647938.1:c.2717A>C	ENSP00000498155.1:p.Asn906Thr
ENST00000674190.1:n.1676A>C
ENST00000319584.10:c.944A>C	ENSP00000313006.6:p.Asn315Thr
ENST00000346085.9:c.2717A>C	ENSP00000344546.4:p.Asn906Thr
ENST00000350026.9:c.2678A>C	ENSP00000055163.7:p.Asn893Thr
ENST00000414678.6:c.1085A>C	ENSP00000412835.2:p.Asn362Thr
ENST00000452544.1:n.774A>C
NM_017519.2:c.2678A>C	NP_059989.2:p.Asn893Thr
NM_020732.3:c.2717A>C	NP_065783.3:p.Asn906Thr
XM_005267069.3:c.2678A>C	XP_005267126.2:p.Asn893Thr
XM_011535984.1:c.1628A>C	XP_011534286.1:p.Asn543Thr
XM_011535985.1:c.1448A>C	XP_011534287.1:p.Asn483Thr
XM_011535986.1:c.1208A>C	XP_011534288.1:p.Asn403Thr
XM_011535987.1:c.827A>C	XP_011534289.1:p.Asn276Thr
XM_011535988.1:c.-20+15582A>C	XP_011534290.1:n.-20+15582A>C
NM_001346813.1:c.2678A>C	NP_001333742.1:p.Asn893Thr
NM_001363725.1:c.428A>C	NP_001350654.1:p.Asn143Thr
XM_011535984.2:c.2759A>C	XP_011534286.2:p.Asn920Thr
XM_011535988.3:c.-20+15582A>C	XP_011534290.1:n.-20+15582A>C
XM_017011103.2:c.2759A>C	XP_016866592.1:p.Asn920Thr
XM_017011104.1:c.2759A>C	XP_016866593.1:p.Asn920Thr
XM_017011105.2:c.2759A>C	XP_016866594.1:p.Asn920Thr
XM_017011106.2:c.2759A>C	XP_016866595.1:p.Asn920Thr
XM_017011107.2:c.2579A>C	XP_016866596.1:p.Asn860Thr
XR_002956289.1:n.2842A>C
NM_001363725.2:c.428A>C	NP_001350654.1:p.Asn143Thr
NM_001371656.1:c.2966A>C	NP_001358585.1:p.Asn989Thr
NM_001374820.1:c.2966A>C	NP_001361749.1:p.Asn989Thr
NM_001374828.1:c.2927A>C MANE Select	NP_001361757.1:p.Asn976Thr
NM_017519.3:c.2927A>C	NP_059989.3:p.Asn976Thr