Canonical Allele Identifier: CA468386260

Gene: FRMD4A MIR1265

Linked Data

• dbSNP Id: rs1367832299
• gnomAD v2: 10-14478609-T-A
• COSMIC: COSN2381254
• MyVariant Identifiers: chr10:g.14478609T>A (hg19) ; chr10:g.14436610T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14436610T>A , CM000672.2:g.14436610T>A	GRCh38
NC_000010.10:g.14478609T>A , CM000672.1:g.14478609T>A	GRCh37
NC_000010.9:g.14518615T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475141.2:c.-305+25458A>T (FRMD4A)	ENSP00000473870.1:n.-305+25458A>T
ENST00000493380.5:c.-82+25458A>T (FRMD4A)	ENSP00000474863.1:n.-82+25458A>T
NR_031668.1:n.35T>A (MIR1265)