Canonical Allele Identifier: CA667221944
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1185163268
gnomAD v3: 10-61985874-G-GA
gnomAD v4: 10-61985874-G-GA
MyVariant Identifiers: chr10:g.63745633_63745634insA (hg19) chr10:g.61985874_61985875insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61985875dup , CM000672.2:g.61985875dup GRCh38
NC_000010.10:g.63745634dup , CM000672.1:g.63745634dup GRCh37
NC_000010.9:g.63415640dup NCBI36
NG_030027.1:g.89622dup

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.503-14216dup MANE Select ENSP00000279873.7:n.503-14216dup
ENST00000644638.1:c.503-14216dup ENSP00000494412.1:n.503-14216dup
ENST00000681100.1:c.503-14216dup ENSP00000506119.1:n.503-14216dup
ENST00000279873.11:c.503-14216dup ENSP00000279873.7:n.503-14216dup
NM_032199.2:c.503-14216dup NP_115575.1:n.503-14216dup
XM_011540262.1:c.502+45467dup XP_011538564.1:n.502+45467dup
XM_024448230.1:c.-65-14216dup XP_024303998.1:n.-65-14216dup
NM_032199.3:c.503-14216dup MANE Select NP_115575.1:n.503-14216dup
Search 100 bp 5'
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