Canonical Allele Identifier: CA2721925530
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs2132852663

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61987941T>G , CM000672.2:g.61987941T>G GRCh38
NC_000010.10:g.63747700T>G , CM000672.1:g.63747700T>G GRCh37
NC_000010.9:g.63417706T>G NCBI36
NG_030027.1:g.91688T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.503-12150T>G MANE Select ENSP00000279873.7:n.503-12150T>G
ENST00000644638.1:c.503-12150T>G ENSP00000494412.1:n.503-12150T>G
ENST00000681100.1:c.503-12150T>G ENSP00000506119.1:n.503-12150T>G
ENST00000279873.11:c.503-12150T>G ENSP00000279873.7:n.503-12150T>G
NM_032199.2:c.503-12150T>G NP_115575.1:n.503-12150T>G
XM_011540262.1:c.502+47533T>G XP_011538564.1:n.502+47533T>G
XM_024448230.1:c.-65-12150T>G XP_024303998.1:n.-65-12150T>G
NM_032199.3:c.503-12150T>G MANE Select NP_115575.1:n.503-12150T>G