Canonical Allele Identifier: CA468386314
Gene: FRMD4A HGNC NCBI
MIR1265 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.14478629T>G (hg19)

Genomic Alleles

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

Transcript Alleles

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