Canonical Allele Identifier: CA1914352007
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1839334500

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62019966T>C , CM000672.2:g.62019966T>C GRCh38
NC_000010.10:g.63779725T>C , CM000672.1:g.63779725T>C GRCh37
NC_000010.9:g.63449731T>C NCBI36
NG_030027.1:g.123713T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.733+19645T>C MANE Select ENSP00000279873.7:n.733+19645T>C
ENST00000644638.1:c.734-4707T>C ENSP00000494412.1:n.734-4707T>C
ENST00000681100.1:c.733+19645T>C ENSP00000506119.1:n.733+19645T>C
ENST00000279873.11:c.733+19645T>C ENSP00000279873.7:n.733+19645T>C
NM_032199.2:c.733+19645T>C NP_115575.1:n.733+19645T>C
XM_011540262.1:c.503-30922T>C XP_011538564.1:n.503-30922T>C
XM_024448230.1:c.166+19645T>C XP_024303998.1:n.166+19645T>C
NM_032199.3:c.733+19645T>C MANE Select NP_115575.1:n.733+19645T>C