Canonical Allele Identifier: CA384491963

Gene: ARID2

Linked Data

• dbSNP Id: rs2138180506
• MyVariant Identifiers: chr12:g.46246456G>A (hg19) ; chr12:g.45852673G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852673G>A , CM000674.2:g.45852673G>A	GRCh38
NC_000012.11:g.46246456G>A , CM000674.1:g.46246456G>A	GRCh37
NC_000012.10:g.44532723G>A	NCBI36
NG_052800.1:g.128009G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4550G>A	ENSP00000415650.3:p.Arg1517Lys
ENST00000457135.2:c.759G>A
ENST00000334344.11:c.4550G>A MANE Select	ENSP00000335044.6:p.Arg1517Lys
ENST00000422737.6:c.4471G>A
ENST00000334344.10:c.4550G>A	ENSP00000335044.6:p.Arg1517Lys
ENST00000422737.5:c.4103G>A	ENSP00000415650.1:p.Arg1368Lys
ENST00000444670.5:c.3380G>A	ENSP00000397307.1:p.Arg1127Lys
ENST00000457135.1:c.374G>A	ENSP00000388357.1:p.Arg125Lys
ENST00000479608.5:n.3841G>A
NM_152641.2:c.4550G>A	NP_689854.2:p.Arg1517Lys
XM_006719272.2:c.4550G>A	XP_006719335.1:p.Arg1517Lys
XM_011538025.1:c.2918G>A	XP_011536327.1:p.Arg973Lys
XR_944505.1:n.4698G>A
NM_001347839.1:c.4550G>A	NP_001334768.1:p.Arg1517Lys
NM_152641.3:c.4550G>A	NP_689854.2:p.Arg1517Lys
XM_006719272.4:c.4550G>A	XP_006719335.1:p.Arg1517Lys
XR_944505.3:n.4681G>A
NM_152641.4:c.4550G>A MANE Select	NP_689854.2:p.Arg1517Lys
NM_001347839.2:c.4550G>A	NP_001334768.1:p.Arg1517Lys