Canonical Allele Identifier: CA662078827
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1450864757
gnomAD v3: 10-14436515-G-A
gnomAD v4: 10-14436515-G-A
MyVariant Identifiers: chr10:g.14478514G>A (hg19) chr10:g.14436515G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436515G>A , CM000672.2:g.14436515G>A GRCh38
NC_000010.10:g.14478514G>A , CM000672.1:g.14478514G>A GRCh37
NC_000010.9:g.14518520G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25553C>T ENSP00000473870.1:n.-305+25553C>T
ENST00000493380.5:c.-82+25553C>T ENSP00000474863.1:n.-82+25553C>T
Search 100 bp 5'
Search 100 bp 3'