Canonical Allele Identifier: CA667222735
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1477954416
MyVariant Identifiers: chr10:g.63747499T>A (hg19) chr10:g.61987740T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61987740T>A , CM000672.2:g.61987740T>A GRCh38
NC_000010.10:g.63747499T>A , CM000672.1:g.63747499T>A GRCh37
NC_000010.9:g.63417505T>A NCBI36
NG_030027.1:g.91487T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-12351T>A MANE Select ENSP00000279873.7:n.503-12351T>A
ENST00000644638.1:c.503-12351T>A ENSP00000494412.1:n.503-12351T>A
ENST00000681100.1:c.503-12351T>A ENSP00000506119.1:n.503-12351T>A
ENST00000279873.11:c.503-12351T>A ENSP00000279873.7:n.503-12351T>A
NM_032199.2:c.503-12351T>A NP_115575.1:n.503-12351T>A
XM_011540262.1:c.502+47332T>A XP_011538564.1:n.502+47332T>A
XM_024448230.1:c.-65-12351T>A XP_024303998.1:n.-65-12351T>A
NM_032199.3:c.503-12351T>A MANE Select NP_115575.1:n.503-12351T>A
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