Canonical Allele Identifier: CA4067750

Gene: ARID1B

Linked Data

• dbSNP Id: rs746048984
• ExAC: 6:157522388 C / T
• gnomAD v2: 6-157522388-C-T
• gnomAD v4: 6-157201254-C-T
• MyVariant Identifiers: chr6:g.157522388C>T (hg19) ; chr6:g.157201254C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201254C>T , CM000668.2:g.157201254C>T	GRCh38
NC_000006.11:g.157522388C>T , CM000668.1:g.157522388C>T	GRCh37
NC_000006.10:g.157564080C>T	NCBI36
NG_032093.1:g.428325C>T
NG_032093.2:g.428325C>T
NG_066624.1:g.430229C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4870C>T	ENSP00000055163.8:p.Pro1624Ser
ENST00000414678.8:c.4939C>T	ENSP00000412835.3:p.Pro1647Ser
ENST00000637015.2:c.5158C>T	ENSP00000489729.2:p.Pro1720Ser
ENST00000346085.10:c.4909C>T	ENSP00000344546.5:p.Pro1637Ser
ENST00000350026.10:c.4621C>T	ENSP00000055163.7:p.Pro1541Ser
ENST00000414678.7:c.3187C>T	ENSP00000412835.2:p.Pro1063Ser
ENST00000635849.1:c.2350C>T	ENSP00000490948.1:p.Pro784Ser
ENST00000635957.1:c.1981C>T	ENSP00000490385.1:p.Pro661Ser
ENST00000636227.1:n.3492C>T
ENST00000636254.1:n.949C>T
ENST00000636930.2:c.5029C>T MANE Select	ENSP00000490491.2:p.Pro1677Ser
ENST00000636940.1:n.3026C>T
ENST00000637015.1:c.2397C>T
ENST00000637568.1:c.2311C>T
ENST00000637741.1:n.1695C>T
ENST00000637810.1:c.2371C>T	ENSP00000489636.1:p.Pro791Ser
ENST00000637904.1:c.2530C>T	ENSP00000490550.1:p.Pro844Ser
ENST00000647938.1:c.4660C>T	ENSP00000498155.1:p.Pro1554Ser
ENST00000346085.9:c.4660C>T	ENSP00000344546.4:p.Pro1554Ser
ENST00000350026.9:c.4621C>T	ENSP00000055163.7:p.Pro1541Ser
ENST00000414678.6:c.3187C>T	ENSP00000412835.2:p.Pro1063Ser
NM_017519.2:c.4621C>T	NP_059989.2:p.Pro1541Ser
NM_020732.3:c.4660C>T	NP_065783.3:p.Pro1554Ser
XM_005267069.3:c.4780C>T	XP_005267126.2:p.Pro1594Ser
XM_011535984.1:c.3859C>T	XP_011534286.1:p.Pro1287Ser
XM_011535985.1:c.3679C>T	XP_011534287.1:p.Pro1227Ser
XM_011535986.1:c.3439C>T	XP_011534288.1:p.Pro1147Ser
XM_011535987.1:c.3058C>T	XP_011534289.1:p.Pro1020Ser
XM_011535988.1:c.1921C>T	XP_011534290.1:p.Pro641Ser
NM_001346813.1:c.4780C>T	NP_001333742.1:p.Pro1594Ser
NM_001363725.1:c.2530C>T	NP_001350654.1:p.Pro844Ser
XM_011535984.2:c.4990C>T	XP_011534286.2:p.Pro1664Ser
XM_011535988.3:c.1921C>T	XP_011534290.1:p.Pro641Ser
XM_017011103.2:c.4891C>T	XP_016866592.1:p.Pro1631Ser
XM_017011104.1:c.4861C>T	XP_016866593.1:p.Pro1621Ser
XM_017011105.2:c.4831C>T	XP_016866594.1:p.Pro1611Ser
XM_017011106.2:c.4702C>T	XP_016866595.1:p.Pro1568Ser
XM_017011107.2:c.4681C>T	XP_016866596.1:p.Pro1561Ser
XR_002956289.1:n.4976C>T
NM_001363725.2:c.2530C>T	NP_001350654.1:p.Pro844Ser
NM_001371656.1:c.4909C>T	NP_001358585.1:p.Pro1637Ser
NM_001374820.1:c.4909C>T	NP_001361749.1:p.Pro1637Ser
NM_001374828.1:c.5029C>T MANE Select	NP_001361757.1:p.Pro1677Ser
NM_017519.3:c.4870C>T	NP_059989.3:p.Pro1624Ser