Canonical Allele Identifier: CA1892118189
Gene: FRMD4A HGNC NCBI
MIR1265 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436597G= , CM000672.2:g.14436597G= GRCh38
NC_000010.10:g.14478596G= , CM000672.1:g.14478596G= GRCh37
NC_000010.9:g.14518602G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25471C= (FRMD4A) ENSP00000473870.1:n.-305+25471C=
ENST00000493380.5:c.-82+25471C= (FRMD4A) ENSP00000474863.1:n.-82+25471C=
NR_031668.1:n.22G= (MIR1265)
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