Canonical Allele Identifier: CA468386333

Gene: FRMD4A MIR1265

Linked Data

• dbSNP Id: rs1483324483
• gnomAD v4: 10-14436635-G-A
• MyVariant Identifiers: chr10:g.14478634G>A (hg19) ; chr10:g.14436635G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14436635G>A , CM000672.2:g.14436635G>A	GRCh38
NC_000010.10:g.14478634G>A , CM000672.1:g.14478634G>A	GRCh37
NC_000010.9:g.14518640G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000475141.2:c.-305+25433C>T (FRMD4A)	ENSP00000473870.1:n.-305+25433C>T
ENST00000493380.5:c.-82+25433C>T (FRMD4A)	ENSP00000474863.1:n.-82+25433C>T
NR_031668.1:n.60G>A (MIR1265)