Canonical Allele Identifier: CA4067497

Gene: ARID1B

Linked Data

• dbSNP Id: rs376806897
• ExAC: 6:157510902 T / C
• gnomAD v2: 6-157510902-T-C
• gnomAD v3: 6-157189768-T-C
• gnomAD v4: 6-157189768-T-C
• MyVariant Identifiers: chr6:g.157510902T>C (hg19) ; chr6:g.157189768T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189768T>C , CM000668.2:g.157189768T>C	GRCh38
NC_000006.11:g.157510902T>C , CM000668.1:g.157510902T>C	GRCh37
NC_000006.10:g.157552594T>C	NCBI36
NG_032093.1:g.416839T>C
NG_032093.2:g.416839T>C
NG_066624.1:g.418743T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3887T>C	ENSP00000055163.8:p.Met1296Thr
ENST00000414678.8:c.3956T>C	ENSP00000412835.3:p.Met1319Thr
ENST00000637015.2:c.4175T>C	ENSP00000489729.2:p.Met1392Thr
ENST00000346085.10:c.3926T>C	ENSP00000344546.5:p.Met1309Thr
ENST00000350026.10:c.3638T>C	ENSP00000055163.7:p.Met1213Thr
ENST00000414678.7:c.2204T>C	ENSP00000412835.2:p.Met735Thr
ENST00000635849.1:c.1367T>C	ENSP00000490948.1:p.Met456Thr
ENST00000635957.1:c.1001T>C	ENSP00000490385.1:p.Met334Thr
ENST00000636930.2:c.4046T>C MANE Select	ENSP00000490491.2:p.Met1349Thr
ENST00000636940.1:n.2043T>C
ENST00000637015.1:c.1414T>C
ENST00000637568.1:c.1328T>C
ENST00000637741.1:n.712T>C
ENST00000637810.1:c.1388T>C	ENSP00000489636.1:p.Met463Thr
ENST00000637904.1:c.1547T>C	ENSP00000490550.1:p.Met516Thr
ENST00000647938.1:c.3677T>C	ENSP00000498155.1:p.Met1226Thr
ENST00000346085.9:c.3677T>C	ENSP00000344546.4:p.Met1226Thr
ENST00000350026.9:c.3638T>C	ENSP00000055163.7:p.Met1213Thr
ENST00000414678.6:c.2204T>C	ENSP00000412835.2:p.Met735Thr
NM_017519.2:c.3638T>C	NP_059989.2:p.Met1213Thr
NM_020732.3:c.3677T>C	NP_065783.3:p.Met1226Thr
XM_005267069.3:c.3797T>C	XP_005267126.2:p.Met1266Thr
XM_011535984.1:c.2876T>C	XP_011534286.1:p.Met959Thr
XM_011535985.1:c.2696T>C	XP_011534287.1:p.Met899Thr
XM_011535986.1:c.2456T>C	XP_011534288.1:p.Met819Thr
XM_011535987.1:c.2075T>C	XP_011534289.1:p.Met692Thr
XM_011535988.1:c.938T>C	XP_011534290.1:p.Met313Thr
NM_001346813.1:c.3797T>C	NP_001333742.1:p.Met1266Thr
NM_001363725.1:c.1547T>C	NP_001350654.1:p.Met516Thr
XM_011535984.2:c.4007T>C	XP_011534286.2:p.Met1336Thr
XM_011535988.3:c.938T>C	XP_011534290.1:p.Met313Thr
XM_017011103.2:c.3908T>C	XP_016866592.1:p.Met1303Thr
XM_017011104.1:c.3878T>C	XP_016866593.1:p.Met1293Thr
XM_017011105.2:c.3848T>C	XP_016866594.1:p.Met1283Thr
XM_017011106.2:c.3719T>C	XP_016866595.1:p.Met1240Thr
XM_017011107.2:c.3698T>C	XP_016866596.1:p.Met1233Thr
XR_002956289.1:n.4090T>C
NM_001363725.2:c.1547T>C	NP_001350654.1:p.Met516Thr
NM_001371656.1:c.3926T>C	NP_001358585.1:p.Met1309Thr
NM_001374820.1:c.3926T>C	NP_001361749.1:p.Met1309Thr
NM_001374828.1:c.4046T>C MANE Select	NP_001361757.1:p.Met1349Thr
NM_017519.3:c.3887T>C	NP_059989.3:p.Met1296Thr