Canonical Allele Identifier: CA2721927700
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs2132889896

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62019980_62019994dup , CM000672.2:g.62019980_62019994dup GRCh38
NC_000010.10:g.63779739_63779753dup , CM000672.1:g.63779739_63779753dup GRCh37
NC_000010.9:g.63449745_63449759dup NCBI36
NG_030027.1:g.123727_123741dup

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.733+19659_733+19673dup MANE Select ENSP00000279873.7:n.733+19659_733+19673dup
ENST00000644638.1:c.734-4693_734-4679dup ENSP00000494412.1:n.734-4693_734-4679dup
ENST00000681100.1:c.733+19659_733+19673dup ENSP00000506119.1:n.733+19659_733+19673dup
ENST00000279873.11:c.733+19659_733+19673dup ENSP00000279873.7:n.733+19659_733+19673dup
NM_032199.2:c.733+19659_733+19673dup NP_115575.1:n.733+19659_733+19673dup
XM_011540262.1:c.503-30908_503-30894dup XP_011538564.1:n.503-30908_503-30894dup
XM_024448230.1:c.166+19659_166+19673dup XP_024303998.1:n.166+19659_166+19673dup
NM_032199.3:c.733+19659_733+19673dup MANE Select NP_115575.1:n.733+19659_733+19673dup