Canonical Allele Identifier: CA366389244

Gene: ARID1B

Linked Data

• dbSNP Id: rs1337652239
• gnomAD v2: 6-157470054-A-G
• gnomAD v4: 6-157148920-A-G
• MyVariant Identifiers: chr6:g.157470054A>G (hg19) ; chr6:g.157148920A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148920A>G , CM000668.2:g.157148920A>G	GRCh38
NC_000006.11:g.157470054A>G , CM000668.1:g.157470054A>G	GRCh37
NC_000006.10:g.157511746A>G	NCBI36
NG_032093.1:g.375991A>G
NG_032093.2:g.375991A>G
NG_066624.1:g.377895A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3058A>G	ENSP00000055163.8:p.Met1020Val
ENST00000414678.8:c.2968A>G	ENSP00000412835.3:p.Met990Val
ENST00000637015.2:c.3058A>G	ENSP00000489729.2:p.Met1020Val
ENST00000319584.11:c.1072A>G	ENSP00000313006.7:p.Met358Val
ENST00000346085.10:c.3097A>G	ENSP00000344546.5:p.Met1033Val
ENST00000350026.10:c.2809A>G	ENSP00000055163.7:p.Met937Val
ENST00000414678.7:c.1216A>G	ENSP00000412835.2:p.Met406Val
ENST00000452544.2:n.959A>G
ENST00000635849.1:c.379A>G	ENSP00000490948.1:p.Met127Val
ENST00000635957.1:c.13A>G	ENSP00000490385.1:p.Met5Val
ENST00000636426.1:n.192A>G
ENST00000636930.2:c.3058A>G MANE Select	ENSP00000490491.2:p.Met1020Val
ENST00000637015.1:c.297A>G
ENST00000637568.1:c.101A>G
ENST00000637810.1:c.559A>G	ENSP00000489636.1:p.Met187Val
ENST00000637904.1:c.559A>G	ENSP00000490550.1:p.Met187Val
ENST00000647938.1:c.2848A>G	ENSP00000498155.1:p.Met950Val
ENST00000674190.1:n.1807A>G
ENST00000319584.10:c.1075A>G	ENSP00000313006.6:p.Met359Val
ENST00000346085.9:c.2848A>G	ENSP00000344546.4:p.Met950Val
ENST00000350026.9:c.2809A>G	ENSP00000055163.7:p.Met937Val
ENST00000400790.3:c.10A>G	ENSP00000383596.3:p.Met4Val
ENST00000414678.6:c.1216A>G	ENSP00000412835.2:p.Met406Val
ENST00000452544.1:n.905A>G
ENST00000478761.3:c.131A>G
NM_017519.2:c.2809A>G	NP_059989.2:p.Met937Val
NM_020732.3:c.2848A>G	NP_065783.3:p.Met950Val
XM_005267069.3:c.2809A>G	XP_005267126.2:p.Met937Val
XM_011535984.1:c.1759A>G	XP_011534286.1:p.Met587Val
XM_011535985.1:c.1579A>G	XP_011534287.1:p.Met527Val
XM_011535986.1:c.1339A>G	XP_011534288.1:p.Met447Val
XM_011535987.1:c.958A>G	XP_011534289.1:p.Met320Val
XM_011535988.1:c.-20+15713A>G	XP_011534290.1:n.-20+15713A>G
NM_001346813.1:c.2809A>G	NP_001333742.1:p.Met937Val
NM_001363725.1:c.559A>G	NP_001350654.1:p.Met187Val
XM_011535984.2:c.2890A>G	XP_011534286.2:p.Met964Val
XM_011535988.3:c.-20+15713A>G	XP_011534290.1:n.-20+15713A>G
XM_017011103.2:c.2890A>G	XP_016866592.1:p.Met964Val
XM_017011104.1:c.2890A>G	XP_016866593.1:p.Met964Val
XM_017011105.2:c.2890A>G	XP_016866594.1:p.Met964Val
XM_017011106.2:c.2890A>G	XP_016866595.1:p.Met964Val
XM_017011107.2:c.2710A>G	XP_016866596.1:p.Met904Val
XR_002956289.1:n.2973A>G
NM_001363725.2:c.559A>G	NP_001350654.1:p.Met187Val
NM_001371656.1:c.3097A>G	NP_001358585.1:p.Met1033Val
NM_001374820.1:c.3097A>G	NP_001361749.1:p.Met1033Val
NM_001374828.1:c.3058A>G MANE Select	NP_001361757.1:p.Met1020Val
NM_017519.3:c.3058A>G	NP_059989.3:p.Met1020Val