Canonical Allele Identifier: CA1914352025
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1839335139

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62020000A>G , CM000672.2:g.62020000A>G GRCh38
NC_000010.10:g.63779759A>G , CM000672.1:g.63779759A>G GRCh37
NC_000010.9:g.63449765A>G NCBI36
NG_030027.1:g.123747A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.733+19679A>G MANE Select ENSP00000279873.7:n.733+19679A>G
ENST00000644638.1:c.734-4673A>G ENSP00000494412.1:n.734-4673A>G
ENST00000681100.1:c.733+19679A>G ENSP00000506119.1:n.733+19679A>G
ENST00000279873.11:c.733+19679A>G ENSP00000279873.7:n.733+19679A>G
NM_032199.2:c.733+19679A>G NP_115575.1:n.733+19679A>G
XM_011540262.1:c.503-30888A>G XP_011538564.1:n.503-30888A>G
XM_024448230.1:c.166+19679A>G XP_024303998.1:n.166+19679A>G
NM_032199.3:c.733+19679A>G MANE Select NP_115575.1:n.733+19679A>G