Canonical Allele Identifier: CA1892118063
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1056549226

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436472C>G , CM000672.2:g.14436472C>G GRCh38
NC_000010.10:g.14478471C>G , CM000672.1:g.14478471C>G GRCh37
NC_000010.9:g.14518477C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25596G>C ENSP00000473870.1:n.-305+25596G>C
ENST00000493380.5:c.-82+25596G>C ENSP00000474863.1:n.-82+25596G>C