Canonical Allele Identifier: CA468386290
Gene: FRMD4A HGNC NCBI
MIR1265 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.14478621A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436622A>C , CM000672.2:g.14436622A>C GRCh38
NC_000010.10:g.14478621A>C , CM000672.1:g.14478621A>C GRCh37
NC_000010.9:g.14518627A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25446T>G (FRMD4A) ENSP00000473870.1:n.-305+25446T>G
ENST00000493380.5:c.-82+25446T>G (FRMD4A) ENSP00000474863.1:n.-82+25446T>G
NR_031668.1:n.47A>C (MIR1265)