Canonical Allele Identifier: CA208309977
Gene: ARID5B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61987926T>C , CM000672.2:g.61987926T>C GRCh38
NC_000010.10:g.63747685T>C , CM000672.1:g.63747685T>C GRCh37
NC_000010.9:g.63417691T>C NCBI36
NG_030027.1:g.91673T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-12165T>C MANE Select ENSP00000279873.7:n.503-12165T>C
ENST00000644638.1:c.503-12165T>C ENSP00000494412.1:n.503-12165T>C
ENST00000681100.1:c.503-12165T>C ENSP00000506119.1:n.503-12165T>C
ENST00000279873.11:c.503-12165T>C ENSP00000279873.7:n.503-12165T>C
NM_032199.2:c.503-12165T>C NP_115575.1:n.503-12165T>C
XM_011540262.1:c.502+47518T>C XP_011538564.1:n.502+47518T>C
XM_024448230.1:c.-65-12165T>C XP_024303998.1:n.-65-12165T>C
NM_032199.3:c.503-12165T>C MANE Select NP_115575.1:n.503-12165T>C
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