Canonical Allele Identifier: CA384492429

Gene: ARID2

Linked Data

• dbSNP Id: rs2138181765
• MyVariant Identifiers: chr12:g.46246614A>C (hg19) ; chr12:g.45852831A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852831A>C , CM000674.2:g.45852831A>C	GRCh38
NC_000012.11:g.46246614A>C , CM000674.1:g.46246614A>C	GRCh37
NC_000012.10:g.44532881A>C	NCBI36
NG_052800.1:g.128167A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4708A>C	ENSP00000415650.3:p.Ile1570Leu
ENST00000457135.2:c.917A>C
ENST00000334344.11:c.4708A>C MANE Select	ENSP00000335044.6:p.Ile1570Leu
ENST00000422737.6:c.4629A>C
ENST00000334344.10:c.4708A>C	ENSP00000335044.6:p.Ile1570Leu
ENST00000422737.5:c.4261A>C	ENSP00000415650.1:p.Ile1421Leu
ENST00000444670.5:c.3538A>C	ENSP00000397307.1:p.Ile1180Leu
ENST00000457135.1:c.532A>C	ENSP00000388357.1:p.Ile178Leu
ENST00000479608.5:n.3999A>C
NM_152641.2:c.4708A>C	NP_689854.2:p.Ile1570Leu
XM_006719272.2:c.4708A>C	XP_006719335.1:p.Ile1570Leu
XM_011538025.1:c.3076A>C	XP_011536327.1:p.Ile1026Leu
XR_944505.1:n.4856A>C
NM_001347839.1:c.4708A>C	NP_001334768.1:p.Ile1570Leu
NM_152641.3:c.4708A>C	NP_689854.2:p.Ile1570Leu
XM_006719272.4:c.4708A>C	XP_006719335.1:p.Ile1570Leu
XR_944505.3:n.4839A>C
NM_152641.4:c.4708A>C MANE Select	NP_689854.2:p.Ile1570Leu
NM_001347839.2:c.4708A>C	NP_001334768.1:p.Ile1570Leu