Canonical Allele Identifier: CA366389236

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148917-G-A
• MyVariant Identifiers: chr6:g.157470051G>A (hg19) ; chr6:g.157148917G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148917G>A , CM000668.2:g.157148917G>A	GRCh38
NC_000006.11:g.157470051G>A , CM000668.1:g.157470051G>A	GRCh37
NC_000006.10:g.157511743G>A	NCBI36
NG_032093.1:g.375988G>A
NG_032093.2:g.375988G>A
NG_066624.1:g.377892G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3055G>A	ENSP00000055163.8:p.Val1019Met
ENST00000414678.8:c.2965G>A	ENSP00000412835.3:p.Val989Met
ENST00000637015.2:c.3055G>A	ENSP00000489729.2:p.Val1019Met
ENST00000319584.11:c.1069G>A	ENSP00000313006.7:p.Val357Met
ENST00000346085.10:c.3094G>A	ENSP00000344546.5:p.Val1032Met
ENST00000350026.10:c.2806G>A	ENSP00000055163.7:p.Val936Met
ENST00000414678.7:c.1213G>A	ENSP00000412835.2:p.Val405Met
ENST00000452544.2:n.956G>A
ENST00000635849.1:c.376G>A	ENSP00000490948.1:p.Val126Met
ENST00000635957.1:c.10G>A	ENSP00000490385.1:p.Val4Met
ENST00000636426.1:n.189G>A
ENST00000636930.2:c.3055G>A MANE Select	ENSP00000490491.2:p.Val1019Met
ENST00000637015.1:c.294G>A
ENST00000637568.1:c.98G>A
ENST00000637810.1:c.556G>A	ENSP00000489636.1:p.Val186Met
ENST00000637904.1:c.556G>A	ENSP00000490550.1:p.Val186Met
ENST00000647938.1:c.2845G>A	ENSP00000498155.1:p.Val949Met
ENST00000674190.1:n.1804G>A
ENST00000319584.10:c.1072G>A	ENSP00000313006.6:p.Val358Met
ENST00000346085.9:c.2845G>A	ENSP00000344546.4:p.Val949Met
ENST00000350026.9:c.2806G>A	ENSP00000055163.7:p.Val936Met
ENST00000400790.3:c.7G>A	ENSP00000383596.3:p.Val3Met
ENST00000414678.6:c.1213G>A	ENSP00000412835.2:p.Val405Met
ENST00000452544.1:n.902G>A
ENST00000478761.3:c.128G>A
NM_017519.2:c.2806G>A	NP_059989.2:p.Val936Met
NM_020732.3:c.2845G>A	NP_065783.3:p.Val949Met
XM_005267069.3:c.2806G>A	XP_005267126.2:p.Val936Met
XM_011535984.1:c.1756G>A	XP_011534286.1:p.Val586Met
XM_011535985.1:c.1576G>A	XP_011534287.1:p.Val526Met
XM_011535986.1:c.1336G>A	XP_011534288.1:p.Val446Met
XM_011535987.1:c.955G>A	XP_011534289.1:p.Val319Met
XM_011535988.1:c.-20+15710G>A	XP_011534290.1:n.-20+15710G>A
NM_001346813.1:c.2806G>A	NP_001333742.1:p.Val936Met
NM_001363725.1:c.556G>A	NP_001350654.1:p.Val186Met
XM_011535984.2:c.2887G>A	XP_011534286.2:p.Val963Met
XM_011535988.3:c.-20+15710G>A	XP_011534290.1:n.-20+15710G>A
XM_017011103.2:c.2887G>A	XP_016866592.1:p.Val963Met
XM_017011104.1:c.2887G>A	XP_016866593.1:p.Val963Met
XM_017011105.2:c.2887G>A	XP_016866594.1:p.Val963Met
XM_017011106.2:c.2887G>A	XP_016866595.1:p.Val963Met
XM_017011107.2:c.2707G>A	XP_016866596.1:p.Val903Met
XR_002956289.1:n.2970G>A
NM_001363725.2:c.556G>A	NP_001350654.1:p.Val186Met
NM_001371656.1:c.3094G>A	NP_001358585.1:p.Val1032Met
NM_001374820.1:c.3094G>A	NP_001361749.1:p.Val1032Met
NM_001374828.1:c.3055G>A MANE Select	NP_001361757.1:p.Val1019Met
NM_017519.3:c.3055G>A	NP_059989.3:p.Val1019Met