Canonical Allele Identifier: CA452780807

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317550
• gnomAD v4: 6-157181124-C-G
• MyVariant Identifiers: chr6:g.157502258C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181124C>G , CM000668.2:g.157181124C>G	GRCh38
NC_000006.11:g.157502258C>G , CM000668.1:g.157502258C>G	GRCh37
NC_000006.10:g.157543950C>G	NCBI36
NG_032093.1:g.408195C>G
NG_032093.2:g.408195C>G
NG_066624.1:g.410099C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3501C>G	ENSP00000055163.8:p.Pro1167=
ENST00000414678.8:c.3570C>G	ENSP00000412835.3:p.Pro1190=
ENST00000637015.2:c.3789C>G	ENSP00000489729.2:p.Pro1263=
ENST00000319584.11:c.1674C>G	ENSP00000313006.7:p.Pro558=
ENST00000346085.10:c.3540C>G	ENSP00000344546.5:p.Pro1180=
ENST00000350026.10:c.3252C>G	ENSP00000055163.7:p.Pro1084=
ENST00000414678.7:c.1818C>G	ENSP00000412835.2:p.Pro606=
ENST00000635849.1:c.981C>G	ENSP00000490948.1:p.Pro327=
ENST00000635957.1:c.615C>G	ENSP00000490385.1:p.Pro205=
ENST00000636930.2:c.3660C>G MANE Select	ENSP00000490491.2:p.Pro1220=
ENST00000636940.1:n.1657C>G
ENST00000637015.1:c.1028C>G
ENST00000637568.1:c.942C>G
ENST00000637741.1:n.326C>G
ENST00000637810.1:c.1002C>G	ENSP00000489636.1:p.Pro334=
ENST00000637904.1:c.1161C>G	ENSP00000490550.1:p.Pro387=
ENST00000647938.1:c.3291C>G	ENSP00000498155.1:p.Pro1097=
ENST00000319584.10:c.1677C>G	ENSP00000313006.6:p.Pro559=
ENST00000346085.9:c.3291C>G	ENSP00000344546.4:p.Pro1097=
ENST00000350026.9:c.3252C>G	ENSP00000055163.7:p.Pro1084=
ENST00000400790.3:c.453C>G	ENSP00000383596.3:p.Pro151=
ENST00000414678.6:c.1818C>G	ENSP00000412835.2:p.Pro606=
ENST00000478761.3:c.862C>G
NM_017519.2:c.3252C>G	NP_059989.2:p.Pro1084=
NM_020732.3:c.3291C>G	NP_065783.3:p.Pro1097=
XM_005267069.3:c.3411C>G	XP_005267126.2:p.Pro1137=
XM_011535984.1:c.2490C>G	XP_011534286.1:p.Pro830=
XM_011535985.1:c.2310C>G	XP_011534287.1:p.Pro770=
XM_011535986.1:c.2070C>G	XP_011534288.1:p.Pro690=
XM_011535987.1:c.1689C>G	XP_011534289.1:p.Pro563=
XM_011535988.1:c.552C>G	XP_011534290.1:p.Pro184=
NM_001346813.1:c.3411C>G	NP_001333742.1:p.Pro1137=
NM_001363725.1:c.1161C>G	NP_001350654.1:p.Pro387=
XM_011535984.2:c.3621C>G	XP_011534286.2:p.Pro1207=
XM_011535988.3:c.552C>G	XP_011534290.1:p.Pro184=
XM_017011103.2:c.3522C>G	XP_016866592.1:p.Pro1174=
XM_017011104.1:c.3492C>G	XP_016866593.1:p.Pro1164=
XM_017011105.2:c.3462C>G	XP_016866594.1:p.Pro1154=
XM_017011106.2:c.3333C>G	XP_016866595.1:p.Pro1111=
XM_017011107.2:c.3312C>G	XP_016866596.1:p.Pro1104=
XR_002956289.1:n.3704C>G
NM_001363725.2:c.1161C>G	NP_001350654.1:p.Pro387=
NM_001371656.1:c.3540C>G	NP_001358585.1:p.Pro1180=
NM_001374820.1:c.3540C>G	NP_001361749.1:p.Pro1180=
NM_001374828.1:c.3660C>G MANE Select	NP_001361757.1:p.Pro1220=
NM_017519.3:c.3501C>G	NP_059989.3:p.Pro1167=