Canonical Allele Identifier: CA1914352002
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1839334256
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62019954C>T , CM000672.2:g.62019954C>T GRCh38
NC_000010.10:g.63779713C>T , CM000672.1:g.63779713C>T GRCh37
NC_000010.9:g.63449719C>T NCBI36
NG_030027.1:g.123701C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.733+19633C>T MANE Select ENSP00000279873.7:n.733+19633C>T
ENST00000644638.1:c.734-4719C>T ENSP00000494412.1:n.734-4719C>T
ENST00000681100.1:c.733+19633C>T ENSP00000506119.1:n.733+19633C>T
ENST00000279873.11:c.733+19633C>T ENSP00000279873.7:n.733+19633C>T
NM_032199.2:c.733+19633C>T NP_115575.1:n.733+19633C>T
XM_011540262.1:c.503-30934C>T XP_011538564.1:n.503-30934C>T
XM_024448230.1:c.166+19633C>T XP_024303998.1:n.166+19633C>T
NM_032199.3:c.733+19633C>T MANE Select NP_115575.1:n.733+19633C>T
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