Canonical Allele Identifier: CA929064379
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1838427184
gnomAD v3: 10-61958663-A-C
gnomAD v4: 10-61958663-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61958663A>C , CM000672.2:g.61958663A>C GRCh38
NC_000010.10:g.63718422A>C , CM000672.1:g.63718422A>C GRCh37
NC_000010.9:g.63388428A>C NCBI36
NG_030027.1:g.62410A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.502+18255A>C MANE Select ENSP00000279873.7:n.502+18255A>C
ENST00000644638.1:c.502+18255A>C ENSP00000494412.1:n.502+18255A>C
ENST00000681100.1:c.502+18255A>C ENSP00000506119.1:n.502+18255A>C
ENST00000279873.11:c.502+18255A>C ENSP00000279873.7:n.502+18255A>C
NM_032199.2:c.502+18255A>C NP_115575.1:n.502+18255A>C
XM_011540262.1:c.502+18255A>C XP_011538564.1:n.502+18255A>C
XM_024448230.1:c.-66+18255A>C XP_024303998.1:n.-66+18255A>C
NM_032199.3:c.502+18255A>C MANE Select NP_115575.1:n.502+18255A>C
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