Canonical Allele Identifier: CA593885162
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1410343620

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61985845A>G , CM000672.2:g.61985845A>G GRCh38
NC_000010.10:g.63745604A>G , CM000672.1:g.63745604A>G GRCh37
NC_000010.9:g.63415610A>G NCBI36
NG_030027.1:g.89592A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.503-14246A>G MANE Select ENSP00000279873.7:n.503-14246A>G
ENST00000644638.1:c.503-14246A>G ENSP00000494412.1:n.503-14246A>G
ENST00000681100.1:c.503-14246A>G ENSP00000506119.1:n.503-14246A>G
ENST00000279873.11:c.503-14246A>G ENSP00000279873.7:n.503-14246A>G
NM_032199.2:c.503-14246A>G NP_115575.1:n.503-14246A>G
XM_011540262.1:c.502+45437A>G XP_011538564.1:n.502+45437A>G
XM_024448230.1:c.-65-14246A>G XP_024303998.1:n.-65-14246A>G
NM_032199.3:c.503-14246A>G MANE Select NP_115575.1:n.503-14246A>G