Canonical Allele Identifier: CA1892118013
Gene: FRMD4A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436409C= , CM000672.2:g.14436409C= GRCh38
NC_000010.10:g.14478408C= , CM000672.1:g.14478408C= GRCh37
NC_000010.9:g.14518414C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25659G= ENSP00000473870.1:n.-305+25659G=
ENST00000493380.5:c.-82+25659G= ENSP00000474863.1:n.-82+25659G=