Canonical Allele Identifier: CA5415015
Gene: FRMD4A HGNC NCBI
MIR1265 HGNC NCBI

Linked Data

dbSNP Id: rs772457871

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436630T>C , CM000672.2:g.14436630T>C GRCh38
NC_000010.10:g.14478629T>C , CM000672.1:g.14478629T>C GRCh37
NC_000010.9:g.14518635T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25438A>G (FRMD4A) ENSP00000473870.1:n.-305+25438A>G
ENST00000493380.5:c.-82+25438A>G (FRMD4A) ENSP00000474863.1:n.-82+25438A>G
NR_031668.1:n.55T>C (MIR1265)