Canonical Allele Identifier: CA592244574
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1315741373

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436548T>C , CM000672.2:g.14436548T>C GRCh38
NC_000010.10:g.14478547T>C , CM000672.1:g.14478547T>C GRCh37
NC_000010.9:g.14518553T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25520A>G ENSP00000473870.1:n.-305+25520A>G
ENST00000493380.5:c.-82+25520A>G ENSP00000474863.1:n.-82+25520A>G