Canonical Allele Identifier: CA208336100
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs921630915
gnomAD v3: 10-62020060-T-C
gnomAD v4: 10-62020060-T-C
MyVariant Identifiers: chr10:g.63779819T>C (hg19) chr10:g.62020060T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62020060T>C , CM000672.2:g.62020060T>C GRCh38
NC_000010.10:g.63779819T>C , CM000672.1:g.63779819T>C GRCh37
NC_000010.9:g.63449825T>C NCBI36
NG_030027.1:g.123807T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.733+19739T>C MANE Select ENSP00000279873.7:n.733+19739T>C
ENST00000644638.1:c.734-4613T>C ENSP00000494412.1:n.734-4613T>C
ENST00000681100.1:c.733+19739T>C ENSP00000506119.1:n.733+19739T>C
ENST00000279873.11:c.733+19739T>C ENSP00000279873.7:n.733+19739T>C
NM_032199.2:c.733+19739T>C NP_115575.1:n.733+19739T>C
XM_011540262.1:c.503-30828T>C XP_011538564.1:n.503-30828T>C
XM_024448230.1:c.166+19739T>C XP_024303998.1:n.166+19739T>C
NM_032199.3:c.733+19739T>C MANE Select NP_115575.1:n.733+19739T>C
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