Canonical Allele Identifier: CA6526700
Gene: ARID2 HGNC NCBI

Linked Data

dbSNP Id: rs745781765

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45852786G>T , CM000674.2:g.45852786G>T GRCh38
NC_000012.11:g.46246569G>T , CM000674.1:g.46246569G>T GRCh37
NC_000012.10:g.44532836G>T NCBI36
NG_052800.1:g.128122G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000422737.7:c.4663G>T ENSP00000415650.3:p.Ala1555Ser
ENST00000457135.2:c.872G>T
ENST00000334344.11:c.4663G>T MANE Select ENSP00000335044.6:p.Ala1555Ser
ENST00000422737.6:c.4584G>T
ENST00000334344.10:c.4663G>T ENSP00000335044.6:p.Ala1555Ser
ENST00000422737.5:c.4216G>T ENSP00000415650.1:p.Ala1406Ser
ENST00000444670.5:c.3493G>T ENSP00000397307.1:p.Ala1165Ser
ENST00000457135.1:c.487G>T ENSP00000388357.1:p.Ala163Ser
ENST00000479608.5:n.3954G>T
NM_152641.2:c.4663G>T NP_689854.2:p.Ala1555Ser
XM_006719272.2:c.4663G>T XP_006719335.1:p.Ala1555Ser
XM_011538025.1:c.3031G>T XP_011536327.1:p.Ala1011Ser
XR_944505.1:n.4811G>T
NM_001347839.1:c.4663G>T NP_001334768.1:p.Ala1555Ser
NM_152641.3:c.4663G>T NP_689854.2:p.Ala1555Ser
XM_006719272.4:c.4663G>T XP_006719335.1:p.Ala1555Ser
XR_944505.3:n.4794G>T
NM_152641.4:c.4663G>T MANE Select NP_689854.2:p.Ala1555Ser
NM_001347839.2:c.4663G>T NP_001334768.1:p.Ala1555Ser