Canonical Allele Identifier: CA1914352055
Gene: ARID5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62020081_62020082delinsGA , CM000672.2:g.62020081_62020082delinsGA GRCh38
NC_000010.10:g.63779840_63779841delinsGA , CM000672.1:g.63779840_63779841delinsGA GRCh37
NC_000010.9:g.63449846_63449847delinsGA NCBI36
NG_030027.1:g.123828_123829delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.733+19760_733+19761delinsGA MANE Select ENSP00000279873.7:n.733+19760_733+19761de...
ENST00000644638.1:c.734-4592_734-4591delinsGA ENSP00000494412.1:n.734-4592_734-4591deli...
ENST00000681100.1:c.733+19760_733+19761delinsGA ENSP00000506119.1:n.733+19760_733+19761de...
ENST00000279873.11:c.733+19760_733+19761delinsGA ENSP00000279873.7:n.733+19760_733+19761de...
NM_032199.2:c.733+19760_733+19761delinsGA NP_115575.1:n.733+19760_733+19761delinsGA...
XM_011540262.1:c.503-30807_503-30806delinsGA XP_011538564.1:n.503-30807_503-30806delin...
XM_024448230.1:c.166+19760_166+19761delinsGA XP_024303998.1:n.166+19760_166+19761delin...
NM_032199.3:c.733+19760_733+19761delinsGA MANE Select NP_115575.1:n.733+19760_733+19761delinsGA...