Canonical Allele Identifier: CA1892118567
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1844564145

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14437061del , CM000672.2:g.14437061del GRCh38
NC_000010.10:g.14479060del , CM000672.1:g.14479060del GRCh37
NC_000010.9:g.14519066del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25007del ENSP00000473870.1:n.-305+25007del
ENST00000493380.5:c.-82+25007del ENSP00000474863.1:n.-82+25007del