Canonical Allele Identifier: CA667212048
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1295598457
gnomAD v3: 10-62020050-A-AC
gnomAD v4: 10-62020050-A-AC
MyVariant Identifiers: chr10:g.63779809_63779810insC (hg19) chr10:g.62020050_62020051insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62020053dup , CM000672.2:g.62020053dup GRCh38
NC_000010.10:g.63779812dup , CM000672.1:g.63779812dup GRCh37
NC_000010.9:g.63449818dup NCBI36
NG_030027.1:g.123800dup

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.733+19732dup MANE Select ENSP00000279873.7:n.733+19732dup
ENST00000644638.1:c.734-4620dup ENSP00000494412.1:n.734-4620dup
ENST00000681100.1:c.733+19732dup ENSP00000506119.1:n.733+19732dup
ENST00000279873.11:c.733+19732dup ENSP00000279873.7:n.733+19732dup
NM_032199.2:c.733+19732dup NP_115575.1:n.733+19732dup
XM_011540262.1:c.503-30835dup XP_011538564.1:n.503-30835dup
XM_024448230.1:c.166+19732dup XP_024303998.1:n.166+19732dup
NM_032199.3:c.733+19732dup MANE Select NP_115575.1:n.733+19732dup
Search 100 bp 5'
Search 100 bp 3'