Canonical Allele Identifier: CA208336113
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs933062386
gnomAD v2: 10-63779823-G-C
gnomAD v3: 10-62020064-G-C
gnomAD v4: 10-62020064-G-C
MyVariant Identifiers: chr10:g.63779823G>C (hg19) chr10:g.62020064G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62020064G>C , CM000672.2:g.62020064G>C GRCh38
NC_000010.10:g.63779823G>C , CM000672.1:g.63779823G>C GRCh37
NC_000010.9:g.63449829G>C NCBI36
NG_030027.1:g.123811G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.733+19743G>C MANE Select ENSP00000279873.7:n.733+19743G>C
ENST00000644638.1:c.734-4609G>C ENSP00000494412.1:n.734-4609G>C
ENST00000681100.1:c.733+19743G>C ENSP00000506119.1:n.733+19743G>C
ENST00000279873.11:c.733+19743G>C ENSP00000279873.7:n.733+19743G>C
NM_032199.2:c.733+19743G>C NP_115575.1:n.733+19743G>C
XM_011540262.1:c.503-30824G>C XP_011538564.1:n.503-30824G>C
XM_024448230.1:c.166+19743G>C XP_024303998.1:n.166+19743G>C
NM_032199.3:c.733+19743G>C MANE Select NP_115575.1:n.733+19743G>C
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