Canonical Allele Identifier: CA1892118080
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1564492365

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436493T>C , CM000672.2:g.14436493T>C GRCh38
NC_000010.10:g.14478492T>C , CM000672.1:g.14478492T>C GRCh37
NC_000010.9:g.14518498T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25575A>G ENSP00000473870.1:n.-305+25575A>G
ENST00000493380.5:c.-82+25575A>G ENSP00000474863.1:n.-82+25575A>G