Canonical Allele Identifier: CA925165153
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1844557173
gnomAD v3: 10-14436437-A-C
gnomAD v4: 10-14436437-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436437A>C , CM000672.2:g.14436437A>C GRCh38
NC_000010.10:g.14478436A>C , CM000672.1:g.14478436A>C GRCh37
NC_000010.9:g.14518442A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25631T>G ENSP00000473870.1:n.-305+25631T>G
ENST00000493380.5:c.-82+25631T>G ENSP00000474863.1:n.-82+25631T>G
Search 100 bp 5'
Search 100 bp 3'