Canonical Allele Identifier: CA1892118168
Gene: FRMD4A HGNC NCBI
MIR1265 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436576A= , CM000672.2:g.14436576A= GRCh38
NC_000010.10:g.14478575A= , CM000672.1:g.14478575A= GRCh37
NC_000010.9:g.14518581A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25492T= (FRMD4A) ENSP00000473870.1:n.-305+25492T=
ENST00000493380.5:c.-82+25492T= (FRMD4A) ENSP00000474863.1:n.-82+25492T=
NR_031668.1:n.1A= (MIR1265)
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