Canonical Allele Identifier: CA13192158
Gene: ARID5B HGNC NCBI
dbSNP:
4948496
gnomAD v2:
10:63805617 T / C
gnomAD v3:
10:62045858 T / C
gnomAD v4:
chr10-62045858-T-C
Joint Max Group AF 0.65083059 (AFR)
Genomes Max Group AF 0.65083059 (AFR)
MyVariant.info:
GRCh38 chr10:g.62045858T>C
GRCh37 chr10:g.63805617T>C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62045858T>C , CM000672.2:g.62045858T>C GRCh38
NC_000010.10:g.63805617T>C , CM000672.1:g.63805617T>C GRCh37
NC_000010.9:g.63475623T>C NCBI36
NG_030027.1:g.149605T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.734-5030T>C MANE Select ENSP00000279873.7:n.734-5030T>C
ENST00000681100.1:c.734-5030T>C ENSP00000506119.1:n.734-5030T>C
ENST00000279873.11:c.734-5030T>C ENSP00000279873.7:n.734-5030T>C
NM_032199.2:c.734-5030T>C NP_115575.1:n.734-5030T>C
XM_011540262.1:c.503-5030T>C XP_011538564.1:n.503-5030T>C
XM_024448230.1:c.167-5030T>C XP_024303998.1:n.167-5030T>C
NM_032199.3:c.734-5030T>C MANE Select NP_115575.1:n.734-5030T>C
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