Canonical Allele Identifier: CA203746030
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs187197691

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436972G>A , CM000672.2:g.14436972G>A GRCh38
NC_000010.10:g.14478971G>A , CM000672.1:g.14478971G>A GRCh37
NC_000010.9:g.14518977G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25096C>T ENSP00000473870.1:n.-305+25096C>T
ENST00000493380.5:c.-82+25096C>T ENSP00000474863.1:n.-82+25096C>T