Canonical Allele Identifier: CA366389306

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148949-C-A
• MyVariant Identifiers: chr6:g.157470083C>A (hg19) ; chr6:g.157148949C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148949C>A , CM000668.2:g.157148949C>A	GRCh38
NC_000006.11:g.157470083C>A , CM000668.1:g.157470083C>A	GRCh37
NC_000006.10:g.157511775C>A	NCBI36
NG_032093.1:g.376020C>A
NG_032093.2:g.376020C>A
NG_066624.1:g.377924C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3087C>A	ENSP00000055163.8:p.Ser1029Arg
ENST00000414678.8:c.2997C>A	ENSP00000412835.3:p.Ser999Arg
ENST00000637015.2:c.3087C>A	ENSP00000489729.2:p.Ser1029Arg
ENST00000319584.11:c.1101C>A	ENSP00000313006.7:p.Ser367Arg
ENST00000346085.10:c.3126C>A	ENSP00000344546.5:p.Ser1042Arg
ENST00000350026.10:c.2838C>A	ENSP00000055163.7:p.Ser946Arg
ENST00000414678.7:c.1245C>A	ENSP00000412835.2:p.Ser415Arg
ENST00000452544.2:n.988C>A
ENST00000635849.1:c.408C>A	ENSP00000490948.1:p.Ser136Arg
ENST00000635957.1:c.42C>A	ENSP00000490385.1:p.Ser14Arg
ENST00000636426.1:n.221C>A
ENST00000636930.2:c.3087C>A MANE Select	ENSP00000490491.2:p.Ser1029Arg
ENST00000637015.1:c.326C>A
ENST00000637568.1:c.130C>A
ENST00000637810.1:c.588C>A	ENSP00000489636.1:p.Ser196Arg
ENST00000637904.1:c.588C>A	ENSP00000490550.1:p.Ser196Arg
ENST00000647938.1:c.2877C>A	ENSP00000498155.1:p.Ser959Arg
ENST00000674190.1:n.1836C>A
ENST00000319584.10:c.1104C>A	ENSP00000313006.6:p.Ser368Arg
ENST00000346085.9:c.2877C>A	ENSP00000344546.4:p.Ser959Arg
ENST00000350026.9:c.2838C>A	ENSP00000055163.7:p.Ser946Arg
ENST00000400790.3:c.39C>A	ENSP00000383596.3:p.Ser13Arg
ENST00000414678.6:c.1245C>A	ENSP00000412835.2:p.Ser415Arg
ENST00000452544.1:n.934C>A
ENST00000478761.3:c.160C>A
NM_017519.2:c.2838C>A	NP_059989.2:p.Ser946Arg
NM_020732.3:c.2877C>A	NP_065783.3:p.Ser959Arg
XM_005267069.3:c.2838C>A	XP_005267126.2:p.Ser946Arg
XM_011535984.1:c.1788C>A	XP_011534286.1:p.Ser596Arg
XM_011535985.1:c.1608C>A	XP_011534287.1:p.Ser536Arg
XM_011535986.1:c.1368C>A	XP_011534288.1:p.Ser456Arg
XM_011535987.1:c.987C>A	XP_011534289.1:p.Ser329Arg
XM_011535988.1:c.-20+15742C>A	XP_011534290.1:n.-20+15742C>A
NM_001346813.1:c.2838C>A	NP_001333742.1:p.Ser946Arg
NM_001363725.1:c.588C>A	NP_001350654.1:p.Ser196Arg
XM_011535984.2:c.2919C>A	XP_011534286.2:p.Ser973Arg
XM_011535988.3:c.-20+15742C>A	XP_011534290.1:n.-20+15742C>A
XM_017011103.2:c.2919C>A	XP_016866592.1:p.Ser973Arg
XM_017011104.1:c.2919C>A	XP_016866593.1:p.Ser973Arg
XM_017011105.2:c.2919C>A	XP_016866594.1:p.Ser973Arg
XM_017011106.2:c.2919C>A	XP_016866595.1:p.Ser973Arg
XM_017011107.2:c.2739C>A	XP_016866596.1:p.Ser913Arg
XR_002956289.1:n.3002C>A
NM_001363725.2:c.588C>A	NP_001350654.1:p.Ser196Arg
NM_001371656.1:c.3126C>A	NP_001358585.1:p.Ser1042Arg
NM_001374820.1:c.3126C>A	NP_001361749.1:p.Ser1042Arg
NM_001374828.1:c.3087C>A MANE Select	NP_001361757.1:p.Ser1029Arg
NM_017519.3:c.3087C>A	NP_059989.3:p.Ser1029Arg