Canonical Allele Identifier: CA150806035

Gene: ARID1B

Linked Data

• dbSNP Id: rs1014389598
• gnomAD v2: 6-157128162-T-C
• gnomAD v3: 6-156807028-T-C
• gnomAD v4: 6-156807028-T-C
• MyVariant Identifiers: chr6:g.157128162T>C (hg19) ; chr6:g.156807028T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156807028T>C , CM000668.2:g.156807028T>C	GRCh38
NC_000006.11:g.157128162T>C , CM000668.1:g.157128162T>C	GRCh37
NC_000006.10:g.157169854T>C	NCBI36
NG_032093.1:g.34099T>C
NG_032093.2:g.34099T>C
NG_066624.1:g.36003T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.1792-22199T>C	ENSP00000055163.8:n.1792-22199T>C
ENST00000414678.8:c.1792-22199T>C	ENSP00000412835.3:n.1792-22199T>C
ENST00000637015.2:c.1792-22199T>C	ENSP00000489729.2:n.1792-22199T>C
ENST00000346085.10:c.1792-22199T>C	ENSP00000344546.5:n.1792-22199T>C
ENST00000350026.10:c.1543-22199T>C	ENSP00000055163.7:n.1543-22199T>C
ENST00000414678.7:c.40-22199T>C	ENSP00000412835.2:n.40-22199T>C
ENST00000494260.2:c.73-22199T>C	ENSP00000490094.1:n.73-22199T>C
ENST00000636607.1:c.55-22199T>C	ENSP00000490050.1:n.55-22199T>C
ENST00000636748.1:c.73-22199T>C	ENSP00000489917.1:n.73-22199T>C
ENST00000636930.2:c.1792-22199T>C MANE Select	ENSP00000490491.2:n.1792-22199T>C
ENST00000637910.1:n.73-22199T>C
ENST00000638000.1:c.9-22199T>C
ENST00000647938.1:c.1543-22199T>C	ENSP00000498155.1:n.1543-22199T>C
ENST00000674190.1:n.499-22199T>C
ENST00000674298.1:c.1532-22199T>C
ENST00000346085.9:c.1543-22199T>C	ENSP00000344546.4:n.1543-22199T>C
ENST00000350026.9:c.1543-22199T>C	ENSP00000055163.7:n.1543-22199T>C
ENST00000414678.6:c.40-22199T>C	ENSP00000412835.2:n.40-22199T>C
NM_017519.2:c.1543-22199T>C	NP_059989.2:n.1543-22199T>C
NM_020732.3:c.1543-22199T>C	NP_065783.3:n.1543-22199T>C
XM_005267069.3:c.1543-22199T>C	XP_005267126.2:n.1543-22199T>C
XM_011535984.1:c.412-22199T>C	XP_011534286.1:n.412-22199T>C
XM_011535985.1:c.412-22199T>C	XP_011534287.1:n.412-22199T>C
NM_001346813.1:c.1543-22199T>C	NP_001333742.1:n.1543-22199T>C
XM_011535984.2:c.1543-22199T>C	XP_011534286.2:n.1543-22199T>C
XM_017011103.2:c.1543-22199T>C	XP_016866592.1:n.1543-22199T>C
XM_017011104.1:c.1543-22199T>C	XP_016866593.1:n.1543-22199T>C
XM_017011105.2:c.1543-22199T>C	XP_016866594.1:n.1543-22199T>C
XM_017011106.2:c.1543-22199T>C	XP_016866595.1:n.1543-22199T>C
XM_017011107.2:c.1543-22199T>C	XP_016866596.1:n.1543-22199T>C
XR_002956289.1:n.1626-22199T>C
NM_001371656.1:c.1792-22199T>C	NP_001358585.1:n.1792-22199T>C
NM_001374820.1:c.1792-22199T>C	NP_001361749.1:n.1792-22199T>C
NM_001374828.1:c.1792-22199T>C MANE Select	NP_001361757.1:n.1792-22199T>C
NM_017519.3:c.1792-22199T>C	NP_059989.3:n.1792-22199T>C