Canonical Allele Identifier: CA662078853

Gene: FRMD4A

Linked Data

• dbSNP Id: rs1338445014
• gnomAD v4: 10-14436537-G-A
• MyVariant Identifiers: chr10:g.14478536G>A (hg19) ; chr10:g.14436537G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14436537G>A , CM000672.2:g.14436537G>A	GRCh38
NC_000010.10:g.14478536G>A , CM000672.1:g.14478536G>A	GRCh37
NC_000010.9:g.14518542G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000475141.2:c.-305+25531C>T	ENSP00000473870.1:n.-305+25531C>T
ENST00000493380.5:c.-82+25531C>T	ENSP00000474863.1:n.-82+25531C>T