Canonical Allele Identifier: CA5415005
Gene: FRMD4A HGNC NCBI
MIR1265 HGNC NCBI

Linked Data

dbSNP Id: rs368618020

Genomic Alleles

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

Transcript Alleles

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