Canonical Allele Identifier: CA5515047
Gene: ARID5B HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.61940136A>C
GRCh37 chr10:g.63699895A>C
gnomAD v2:
10:63699895 A / C
gnomAD v3:
10:61940136 A / C
gnomAD v4:
chr10-61940136-A-C
Joint Max Group AF 0.71673106 (AFR)
Genomes Max Group AF 0.71320637 (AFR)
Exomes Max Group AF 0.71642339 (AFR)
dbSNP:
7073837
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61940136A>C , CM000672.2:g.61940136A>C GRCh38
NC_000010.10:g.63699895A>C , CM000672.1:g.63699895A>C GRCh37
NC_000010.9:g.63369901A>C NCBI36
NG_030027.1:g.43883A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.277-47A>C MANE Select ENSP00000279873.7:n.277-47A>C
ENST00000644638.1:c.277-47A>C ENSP00000494412.1:n.277-47A>C
ENST00000681100.1:c.277-47A>C ENSP00000506119.1:n.277-47A>C
ENST00000279873.11:c.277-47A>C ENSP00000279873.7:n.277-47A>C
NM_032199.2:c.277-47A>C NP_115575.1:n.277-47A>C
XM_011540262.1:c.277-47A>C XP_011538564.1:n.277-47A>C
XM_024448230.1:c.-291-47A>C XP_024303998.1:n.-291-47A>C
NM_032199.3:c.277-47A>C MANE Select NP_115575.1:n.277-47A>C
Search 100 bp 5'
Search 100 bp 3'