Canonical Allele Identifier: CA1914339227
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1838939220
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61992436T>A , CM000672.2:g.61992436T>A GRCh38
NC_000010.10:g.63752195T>A , CM000672.1:g.63752195T>A GRCh37
NC_000010.9:g.63422201T>A NCBI36
NG_030027.1:g.96183T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.503-7655T>A MANE Select ENSP00000279873.7:n.503-7655T>A
ENST00000644638.1:c.503-7655T>A ENSP00000494412.1:n.503-7655T>A
ENST00000681100.1:c.503-7655T>A ENSP00000506119.1:n.503-7655T>A
ENST00000279873.11:c.503-7655T>A ENSP00000279873.7:n.503-7655T>A
NM_032199.2:c.503-7655T>A NP_115575.1:n.503-7655T>A
XM_011540262.1:c.502+52028T>A XP_011538564.1:n.502+52028T>A
XM_024448230.1:c.-65-7655T>A XP_024303998.1:n.-65-7655T>A
NM_032199.3:c.503-7655T>A MANE Select NP_115575.1:n.503-7655T>A
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