Canonical Allele Identifier: CA208336250
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1046526301
MyVariant Identifiers: chr10:g.63779990A>G (hg19) chr10:g.62020231A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62020231A>G , CM000672.2:g.62020231A>G GRCh38
NC_000010.10:g.63779990A>G , CM000672.1:g.63779990A>G GRCh37
NC_000010.9:g.63449996A>G NCBI36
NG_030027.1:g.123978A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.733+19910A>G MANE Select ENSP00000279873.7:n.733+19910A>G
ENST00000644638.1:c.734-4442A>G ENSP00000494412.1:n.734-4442A>G
ENST00000681100.1:c.733+19910A>G ENSP00000506119.1:n.733+19910A>G
ENST00000279873.11:c.733+19910A>G ENSP00000279873.7:n.733+19910A>G
NM_032199.2:c.733+19910A>G NP_115575.1:n.733+19910A>G
XM_011540262.1:c.503-30657A>G XP_011538564.1:n.503-30657A>G
XM_024448230.1:c.166+19910A>G XP_024303998.1:n.166+19910A>G
NM_032199.3:c.733+19910A>G MANE Select NP_115575.1:n.733+19910A>G
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