Canonical Allele Identifier: CA366389148

Gene: ARID1B

Linked Data

• dbSNP Id: rs1244548014
• gnomAD v2: 6-157470010-T-C
• gnomAD v4: 6-157148876-T-C
• MyVariant Identifiers: chr6:g.157470010T>C (hg19) ; chr6:g.157148876T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148876T>C , CM000668.2:g.157148876T>C	GRCh38
NC_000006.11:g.157470010T>C , CM000668.1:g.157470010T>C	GRCh37
NC_000006.10:g.157511702T>C	NCBI36
NG_032093.1:g.375947T>C
NG_032093.2:g.375947T>C
NG_066624.1:g.377851T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3014T>C	ENSP00000055163.8:p.Met1005Thr
ENST00000414678.8:c.2924T>C	ENSP00000412835.3:p.Met975Thr
ENST00000637015.2:c.3014T>C	ENSP00000489729.2:p.Met1005Thr
ENST00000319584.11:c.1028T>C	ENSP00000313006.7:p.Met343Thr
ENST00000346085.10:c.3053T>C	ENSP00000344546.5:p.Met1018Thr
ENST00000350026.10:c.2765T>C	ENSP00000055163.7:p.Met922Thr
ENST00000414678.7:c.1172T>C	ENSP00000412835.2:p.Met391Thr
ENST00000452544.2:n.915T>C
ENST00000635849.1:c.335T>C	ENSP00000490948.1:p.Met112Thr
ENST00000636426.1:n.148T>C
ENST00000636930.2:c.3014T>C MANE Select	ENSP00000490491.2:p.Met1005Thr
ENST00000637015.1:c.253T>C
ENST00000637568.1:c.57T>C
ENST00000637810.1:c.515T>C	ENSP00000489636.1:p.Met172Thr
ENST00000637904.1:c.515T>C	ENSP00000490550.1:p.Met172Thr
ENST00000647938.1:c.2804T>C	ENSP00000498155.1:p.Met935Thr
ENST00000674190.1:n.1763T>C
ENST00000319584.10:c.1031T>C	ENSP00000313006.6:p.Met344Thr
ENST00000346085.9:c.2804T>C	ENSP00000344546.4:p.Met935Thr
ENST00000350026.9:c.2765T>C	ENSP00000055163.7:p.Met922Thr
ENST00000414678.6:c.1172T>C	ENSP00000412835.2:p.Met391Thr
ENST00000452544.1:n.861T>C
ENST00000478761.3:c.87T>C
NM_017519.2:c.2765T>C	NP_059989.2:p.Met922Thr
NM_020732.3:c.2804T>C	NP_065783.3:p.Met935Thr
XM_005267069.3:c.2765T>C	XP_005267126.2:p.Met922Thr
XM_011535984.1:c.1715T>C	XP_011534286.1:p.Met572Thr
XM_011535985.1:c.1535T>C	XP_011534287.1:p.Met512Thr
XM_011535986.1:c.1295T>C	XP_011534288.1:p.Met432Thr
XM_011535987.1:c.914T>C	XP_011534289.1:p.Met305Thr
XM_011535988.1:c.-20+15669T>C	XP_011534290.1:n.-20+15669T>C
NM_001346813.1:c.2765T>C	NP_001333742.1:p.Met922Thr
NM_001363725.1:c.515T>C	NP_001350654.1:p.Met172Thr
XM_011535984.2:c.2846T>C	XP_011534286.2:p.Met949Thr
XM_011535988.3:c.-20+15669T>C	XP_011534290.1:n.-20+15669T>C
XM_017011103.2:c.2846T>C	XP_016866592.1:p.Met949Thr
XM_017011104.1:c.2846T>C	XP_016866593.1:p.Met949Thr
XM_017011105.2:c.2846T>C	XP_016866594.1:p.Met949Thr
XM_017011106.2:c.2846T>C	XP_016866595.1:p.Met949Thr
XM_017011107.2:c.2666T>C	XP_016866596.1:p.Met889Thr
XR_002956289.1:n.2929T>C
NM_001363725.2:c.515T>C	NP_001350654.1:p.Met172Thr
NM_001371656.1:c.3053T>C	NP_001358585.1:p.Met1018Thr
NM_001374820.1:c.3053T>C	NP_001361749.1:p.Met1018Thr
NM_001374828.1:c.3014T>C MANE Select	NP_001361757.1:p.Met1005Thr
NM_017519.3:c.3014T>C	NP_059989.3:p.Met1005Thr