Canonical Allele Identifier: CA925165216
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1844559016

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436554T>G , CM000672.2:g.14436554T>G GRCh38
NC_000010.10:g.14478553T>G , CM000672.1:g.14478553T>G GRCh37
NC_000010.9:g.14518559T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25514A>C ENSP00000473870.1:n.-305+25514A>C
ENST00000493380.5:c.-82+25514A>C ENSP00000474863.1:n.-82+25514A>C