Canonical Allele Identifier: CA929076319
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1589249497

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61992051T>A , CM000672.2:g.61992051T>A GRCh38
NC_000010.10:g.63751810T>A , CM000672.1:g.63751810T>A GRCh37
NC_000010.9:g.63421816T>A NCBI36
NG_030027.1:g.95798T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-8040T>A MANE Select ENSP00000279873.7:n.503-8040T>A
ENST00000644638.1:c.503-8040T>A ENSP00000494412.1:n.503-8040T>A
ENST00000681100.1:c.503-8040T>A ENSP00000506119.1:n.503-8040T>A
ENST00000279873.11:c.503-8040T>A ENSP00000279873.7:n.503-8040T>A
NM_032199.2:c.503-8040T>A NP_115575.1:n.503-8040T>A
XM_011540262.1:c.502+51643T>A XP_011538564.1:n.502+51643T>A
XM_024448230.1:c.-65-8040T>A XP_024303998.1:n.-65-8040T>A
NM_032199.3:c.503-8040T>A MANE Select NP_115575.1:n.503-8040T>A