Canonical Allele Identifier: CA208313025
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs372912200
gnomAD v2: 10-63751791-CA-C
gnomAD v3: 10-61992032-CA-C
gnomAD v4: 10-61992032-CA-C
MyVariant Identifiers: chr10:g.63751793del (hg19) chr10:g.63751792del (hg19) chr10:g.61992034del (hg38) chr10:g.61992033del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61992045del , CM000672.2:g.61992045del GRCh38
NC_000010.10:g.63751804del , CM000672.1:g.63751804del GRCh37
NC_000010.9:g.63421810del NCBI36
NG_030027.1:g.95792del

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-8046del MANE Select ENSP00000279873.7:n.503-8046del
ENST00000644638.1:c.503-8046del ENSP00000494412.1:n.503-8046del
ENST00000681100.1:c.503-8046del ENSP00000506119.1:n.503-8046del
ENST00000279873.11:c.503-8046del ENSP00000279873.7:n.503-8046del
NM_032199.2:c.503-8046del NP_115575.1:n.503-8046del
XM_011540262.1:c.502+51637del XP_011538564.1:n.502+51637del
XM_024448230.1:c.-65-8046del XP_024303998.1:n.-65-8046del
NM_032199.3:c.503-8046del MANE Select NP_115575.1:n.503-8046del
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