Canonical Allele Identifier: CA203745854
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs938055526
gnomAD v3: 10-14436404-G-C
gnomAD v4: 10-14436404-G-C
MyVariant Identifiers: chr10:g.14478403G>C (hg19) chr10:g.14436404G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436404G>C , CM000672.2:g.14436404G>C GRCh38
NC_000010.10:g.14478403G>C , CM000672.1:g.14478403G>C GRCh37
NC_000010.9:g.14518409G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25664C>G ENSP00000473870.1:n.-305+25664C>G
ENST00000493380.5:c.-82+25664C>G ENSP00000474863.1:n.-82+25664C>G
Search 100 bp 5'
Search 100 bp 3'