Canonical Allele Identifier: CA468386170
Gene: FRMD4A HGNC NCBI
MIR1265 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.14478578G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436579G>T , CM000672.2:g.14436579G>T GRCh38
NC_000010.10:g.14478578G>T , CM000672.1:g.14478578G>T GRCh37
NC_000010.9:g.14518584G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25489C>A (FRMD4A) ENSP00000473870.1:n.-305+25489C>A
ENST00000493380.5:c.-82+25489C>A (FRMD4A) ENSP00000474863.1:n.-82+25489C>A
NR_031668.1:n.4G>T (MIR1265)