Canonical Allele Identifier: CA1914339027
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1838935432

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61992179_61992180insTTCATAATCC , CM000672.2:g.61992179_61992180insTTCATAATCC GRCh38
NC_000010.10:g.63751938_63751939insTTCATAATCC , CM000672.1:g.63751938_63751939insTTCATAATCC GRCh37
NC_000010.9:g.63421944_63421945insTTCATAATCC NCBI36
NG_030027.1:g.95926_95927insTTCATAATCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-7912_503-7911insTTCATAATCC MANE Select ENSP00000279873.7:n.503-7912_503-7911insTTCATAATCC
ENST00000644638.1:c.503-7912_503-7911insTTCATAATCC ENSP00000494412.1:n.503-7912_503-7911insTTCATAATCC
ENST00000681100.1:c.503-7912_503-7911insTTCATAATCC ENSP00000506119.1:n.503-7912_503-7911insTTCATAATCC
ENST00000279873.11:c.503-7912_503-7911insTTCATAATCC ENSP00000279873.7:n.503-7912_503-7911insTTCATAATCC
NM_032199.2:c.503-7912_503-7911insTTCATAATCC NP_115575.1:n.503-7912_503-7911insTTCATAATCC
XM_011540262.1:c.502+51771_502+51772insTTCATAATCC XP_011538564.1:n.502+51771_502+51772insTTCATAATCC
XM_024448230.1:c.-65-7912_-65-7911insTTCATAATCC XP_024303998.1:n.-65-7912_-65-7911insTTCATAATCC
NM_032199.3:c.503-7912_503-7911insTTCATAATCC MANE Select NP_115575.1:n.503-7912_503-7911insTTCATAATCC