Canonical Allele Identifier: CA1914314664
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1844277440
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61935151A>G , CM000672.2:g.61935151A>G GRCh38
NC_000010.10:g.63694910A>G , CM000672.1:g.63694910A>G GRCh37
NC_000010.9:g.63364916A>G NCBI36
NG_030027.1:g.38898A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.277-5032A>G MANE Select ENSP00000279873.7:n.277-5032A>G
ENST00000644638.1:c.277-5032A>G ENSP00000494412.1:n.277-5032A>G
ENST00000681100.1:c.277-5032A>G ENSP00000506119.1:n.277-5032A>G
ENST00000279873.11:c.277-5032A>G ENSP00000279873.7:n.277-5032A>G
NM_032199.2:c.277-5032A>G NP_115575.1:n.277-5032A>G
XM_011540262.1:c.277-5032A>G XP_011538564.1:n.277-5032A>G
XM_024448230.1:c.-291-5032A>G XP_024303998.1:n.-291-5032A>G
NM_032199.3:c.277-5032A>G MANE Select NP_115575.1:n.277-5032A>G
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