Canonical Allele Identifier: CA4067171

Gene: ARID1B

Linked Data

• dbSNP Id: rs752405476
• ExAC: 6:157469974 T / C
• gnomAD v2: 6-157469974-T-C
• gnomAD v4: 6-157148840-T-C
• MyVariant Identifiers: chr6:g.157469974T>C (hg19) ; chr6:g.157148840T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148840T>C , CM000668.2:g.157148840T>C	GRCh38
NC_000006.11:g.157469974T>C , CM000668.1:g.157469974T>C	GRCh37
NC_000006.10:g.157511666T>C	NCBI36
NG_032093.1:g.375911T>C
NG_032093.2:g.375911T>C
NG_066624.1:g.377815T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2978T>C	ENSP00000055163.8:p.Met993Thr
ENST00000414678.8:c.2888T>C	ENSP00000412835.3:p.Met963Thr
ENST00000637015.2:c.2978T>C	ENSP00000489729.2:p.Met993Thr
ENST00000319584.11:c.992T>C	ENSP00000313006.7:p.Met331Thr
ENST00000346085.10:c.3017T>C	ENSP00000344546.5:p.Met1006Thr
ENST00000350026.10:c.2729T>C	ENSP00000055163.7:p.Met910Thr
ENST00000414678.7:c.1136T>C	ENSP00000412835.2:p.Met379Thr
ENST00000452544.2:n.879T>C
ENST00000635849.1:c.299T>C	ENSP00000490948.1:p.Met100Thr
ENST00000636426.1:n.112T>C
ENST00000636930.2:c.2978T>C MANE Select	ENSP00000490491.2:p.Met993Thr
ENST00000637015.1:c.217T>C
ENST00000637568.1:c.21T>C
ENST00000637810.1:c.479T>C	ENSP00000489636.1:p.Met160Thr
ENST00000637904.1:c.479T>C	ENSP00000490550.1:p.Met160Thr
ENST00000647938.1:c.2768T>C	ENSP00000498155.1:p.Met923Thr
ENST00000674190.1:n.1727T>C
ENST00000319584.10:c.995T>C	ENSP00000313006.6:p.Met332Thr
ENST00000346085.9:c.2768T>C	ENSP00000344546.4:p.Met923Thr
ENST00000350026.9:c.2729T>C	ENSP00000055163.7:p.Met910Thr
ENST00000414678.6:c.1136T>C	ENSP00000412835.2:p.Met379Thr
ENST00000452544.1:n.825T>C
ENST00000478761.3:c.51T>C
NM_017519.2:c.2729T>C	NP_059989.2:p.Met910Thr
NM_020732.3:c.2768T>C	NP_065783.3:p.Met923Thr
XM_005267069.3:c.2729T>C	XP_005267126.2:p.Met910Thr
XM_011535984.1:c.1679T>C	XP_011534286.1:p.Met560Thr
XM_011535985.1:c.1499T>C	XP_011534287.1:p.Met500Thr
XM_011535986.1:c.1259T>C	XP_011534288.1:p.Met420Thr
XM_011535987.1:c.878T>C	XP_011534289.1:p.Met293Thr
XM_011535988.1:c.-20+15633T>C	XP_011534290.1:n.-20+15633T>C
NM_001346813.1:c.2729T>C	NP_001333742.1:p.Met910Thr
NM_001363725.1:c.479T>C	NP_001350654.1:p.Met160Thr
XM_011535984.2:c.2810T>C	XP_011534286.2:p.Met937Thr
XM_011535988.3:c.-20+15633T>C	XP_011534290.1:n.-20+15633T>C
XM_017011103.2:c.2810T>C	XP_016866592.1:p.Met937Thr
XM_017011104.1:c.2810T>C	XP_016866593.1:p.Met937Thr
XM_017011105.2:c.2810T>C	XP_016866594.1:p.Met937Thr
XM_017011106.2:c.2810T>C	XP_016866595.1:p.Met937Thr
XM_017011107.2:c.2630T>C	XP_016866596.1:p.Met877Thr
XR_002956289.1:n.2893T>C
NM_001363725.2:c.479T>C	NP_001350654.1:p.Met160Thr
NM_001371656.1:c.3017T>C	NP_001358585.1:p.Met1006Thr
NM_001374820.1:c.3017T>C	NP_001361749.1:p.Met1006Thr
NM_001374828.1:c.2978T>C MANE Select	NP_001361757.1:p.Met993Thr
NM_017519.3:c.2978T>C	NP_059989.3:p.Met993Thr