Canonical Allele Identifier: CA667224906
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1414699363
MyVariant Identifiers: chr10:g.63751843_63751844insG (hg19) chr10:g.61992084_61992085insG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61992088dup , CM000672.2:g.61992088dup GRCh38
NC_000010.10:g.63751847dup , CM000672.1:g.63751847dup GRCh37
NC_000010.9:g.63421853dup NCBI36
NG_030027.1:g.95835dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-8003dup MANE Select ENSP00000279873.7:n.503-8003dup
ENST00000644638.1:c.503-8003dup ENSP00000494412.1:n.503-8003dup
ENST00000681100.1:c.503-8003dup ENSP00000506119.1:n.503-8003dup
ENST00000279873.11:c.503-8003dup ENSP00000279873.7:n.503-8003dup
NM_032199.2:c.503-8003dup NP_115575.1:n.503-8003dup
XM_011540262.1:c.502+51680dup XP_011538564.1:n.502+51680dup
XM_024448230.1:c.-65-8003dup XP_024303998.1:n.-65-8003dup
NM_032199.3:c.503-8003dup MANE Select NP_115575.1:n.503-8003dup
Search 100 bp 5'
Search 100 bp 3'