Canonical Allele Identifier: CA5414992
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs776303762

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436526G>A , CM000672.2:g.14436526G>A GRCh38
NC_000010.10:g.14478525G>A , CM000672.1:g.14478525G>A GRCh37
NC_000010.9:g.14518531G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25542C>T ENSP00000473870.1:n.-305+25542C>T
ENST00000493380.5:c.-82+25542C>T ENSP00000474863.1:n.-82+25542C>T