Canonical Allele Identifier: CA1914339032
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1838935553

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61992184dup , CM000672.2:g.61992184dup GRCh38
NC_000010.10:g.63751943dup , CM000672.1:g.63751943dup GRCh37
NC_000010.9:g.63421949dup NCBI36
NG_030027.1:g.95931dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-7907dup MANE Select ENSP00000279873.7:n.503-7907dup
ENST00000644638.1:c.503-7907dup ENSP00000494412.1:n.503-7907dup
ENST00000681100.1:c.503-7907dup ENSP00000506119.1:n.503-7907dup
ENST00000279873.11:c.503-7907dup ENSP00000279873.7:n.503-7907dup
NM_032199.2:c.503-7907dup NP_115575.1:n.503-7907dup
XM_011540262.1:c.502+51776dup XP_011538564.1:n.502+51776dup
XM_024448230.1:c.-65-7907dup XP_024303998.1:n.-65-7907dup
NM_032199.3:c.503-7907dup MANE Select NP_115575.1:n.503-7907dup