Canonical Allele Identifier: CA667211181
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1377658238
gnomAD v3: 10-61963326-TA-T
gnomAD v4: 10-61963326-TA-T
MyVariant Identifiers: chr10:g.63723086del (hg19) chr10:g.61963327del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61963331del , CM000672.2:g.61963331del GRCh38
NC_000010.10:g.63723090del , CM000672.1:g.63723090del GRCh37
NC_000010.9:g.63393096del NCBI36
NG_030027.1:g.67078del

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.502+22923del MANE Select ENSP00000279873.7:n.502+22923del
ENST00000644638.1:c.502+22923del ENSP00000494412.1:n.502+22923del
ENST00000681100.1:c.502+22923del ENSP00000506119.1:n.502+22923del
ENST00000279873.11:c.502+22923del ENSP00000279873.7:n.502+22923del
NM_032199.2:c.502+22923del NP_115575.1:n.502+22923del
XM_011540262.1:c.502+22923del XP_011538564.1:n.502+22923del
XM_024448230.1:c.-66+22923del XP_024303998.1:n.-66+22923del
NM_032199.3:c.502+22923del MANE Select NP_115575.1:n.502+22923del
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