Canonical Allele Identifier: CA593885763
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1416690451
gnomAD v2: 10-63752166-G-GT
gnomAD v3: 10-61992407-G-GT
gnomAD v4: 10-61992407-G-GT
MyVariant Identifiers: chr10:g.63752166_63752167insT (hg19) chr10:g.61992407_61992408insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61992415dup , CM000672.2:g.61992415dup GRCh38
NC_000010.10:g.63752174dup , CM000672.1:g.63752174dup GRCh37
NC_000010.9:g.63422180dup NCBI36
NG_030027.1:g.96162dup

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.503-7676dup MANE Select ENSP00000279873.7:n.503-7676dup
ENST00000644638.1:c.503-7676dup ENSP00000494412.1:n.503-7676dup
ENST00000681100.1:c.503-7676dup ENSP00000506119.1:n.503-7676dup
ENST00000279873.11:c.503-7676dup ENSP00000279873.7:n.503-7676dup
NM_032199.2:c.503-7676dup NP_115575.1:n.503-7676dup
XM_011540262.1:c.502+52007dup XP_011538564.1:n.502+52007dup
XM_024448230.1:c.-65-7676dup XP_024303998.1:n.-65-7676dup
NM_032199.3:c.503-7676dup MANE Select NP_115575.1:n.503-7676dup
Search 100 bp 5'
Search 100 bp 3'