Canonical Allele Identifier: CA5415026
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs542508900

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436690A>G , CM000672.2:g.14436690A>G GRCh38
NC_000010.10:g.14478689A>G , CM000672.1:g.14478689A>G GRCh37
NC_000010.9:g.14518695A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25378T>C ENSP00000473870.1:n.-305+25378T>C
ENST00000493380.5:c.-82+25378T>C ENSP00000474863.1:n.-82+25378T>C