Canonical Allele Identifier: CA594019923
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1241272209
gnomAD v2: 10-63723112-GC-G
gnomAD v3: 10-61963353-GC-G
gnomAD v4: 10-61963353-GC-G
MyVariant Identifiers: chr10:g.63723113del (hg19) chr10:g.61963354del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61963356del , CM000672.2:g.61963356del GRCh38
NC_000010.10:g.63723115del , CM000672.1:g.63723115del GRCh37
NC_000010.9:g.63393121del NCBI36
NG_030027.1:g.67103del

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.502+22948del MANE Select ENSP00000279873.7:n.502+22948del
ENST00000644638.1:c.502+22948del ENSP00000494412.1:n.502+22948del
ENST00000681100.1:c.502+22948del ENSP00000506119.1:n.502+22948del
ENST00000279873.11:c.502+22948del ENSP00000279873.7:n.502+22948del
NM_032199.2:c.502+22948del NP_115575.1:n.502+22948del
XM_011540262.1:c.502+22948del XP_011538564.1:n.502+22948del
XM_024448230.1:c.-66+22948del XP_024303998.1:n.-66+22948del
NM_032199.3:c.502+22948del MANE Select NP_115575.1:n.502+22948del
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