Canonical Allele Identifier: CA54126318
Gene: MIR4435-2HG HGNC NCBI

Linked Data

dbSNP Id: rs2271404

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111246290T>C , CM000664.2:g.111246290T>C GRCh38
NC_000002.11:g.112003867T>C , CM000664.1:g.112003867T>C GRCh37
NC_000002.10:g.111720338T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512259.1:c.-309+1858A>G XP_011510561.1:n.-309+1858A>G
XM_011512260.1:c.-114+1858A>G XP_011510562.1:n.-114+1858A>G
XM_011512261.1:c.-2+1858A>G XP_011510563.1:n.-2+1858A>G
NR_015395.2:n.2470-6294A>G
NR_136161.1:n.637+1858A>G
NR_136162.1:n.2470-12551A>G
NR_136163.1:n.637+1858A>G
NR_136164.1:n.544-37629A>G
NR_136165.1:n.548+1858A>G
NR_136166.1:n.2470-12551A>G