Canonical Allele Identifier: CA929076928
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1844278591

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61935219G>A , CM000672.2:g.61935219G>A GRCh38
NC_000010.10:g.63694978G>A , CM000672.1:g.63694978G>A GRCh37
NC_000010.9:g.63364984G>A NCBI36
NG_030027.1:g.38966G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.277-4964G>A MANE Select ENSP00000279873.7:n.277-4964G>A
ENST00000644638.1:c.277-4964G>A ENSP00000494412.1:n.277-4964G>A
ENST00000681100.1:c.277-4964G>A ENSP00000506119.1:n.277-4964G>A
ENST00000279873.11:c.277-4964G>A ENSP00000279873.7:n.277-4964G>A
NM_032199.2:c.277-4964G>A NP_115575.1:n.277-4964G>A
XM_011540262.1:c.277-4964G>A XP_011538564.1:n.277-4964G>A
XM_024448230.1:c.-291-4964G>A XP_024303998.1:n.-291-4964G>A
NM_032199.3:c.277-4964G>A MANE Select NP_115575.1:n.277-4964G>A