Canonical Allele Identifier: CA11024676
Gene: MIR4435-2HG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111231795T>G , CM000664.2:g.111231795T>G GRCh38
NC_000002.11:g.111989372T>G , CM000664.1:g.111989372T>G GRCh37
NC_000002.10:g.111705843T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512259.1:c.-3+1834A>C XP_011510561.1:n.-3+1834A>C
XM_011512260.1:c.-3+1834A>C XP_011510562.1:n.-3+1834A>C
XM_011512261.1:c.-1-6581A>C XP_011510563.1:n.-1-6581A>C
NR_015395.2:n.2776+1833A>C
NR_136161.1:n.749+1833A>C
NR_136162.1:n.2581+1833A>C
NR_136163.1:n.944+1833A>C
NR_136164.1:n.544-23134A>C
NR_136165.1:n.548+16353A>C
NR_136166.1:n.2581+1833A>C
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