Canonical Allele Identifier: CA203745940

Gene: FRMD4A MIR1265

Linked Data

• dbSNP Id: rs11259096
• MyVariant Identifiers: chr10:g.14478618T>G (hg19) ; chr10:g.14436619T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14436619T>G , CM000672.2:g.14436619T>G	GRCh38
NC_000010.10:g.14478618T>G , CM000672.1:g.14478618T>G	GRCh37
NC_000010.9:g.14518624T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000475141.2:c.-305+25449A>C (FRMD4A)	ENSP00000473870.1:n.-305+25449A>C
ENST00000493380.5:c.-82+25449A>C (FRMD4A)	ENSP00000474863.1:n.-82+25449A>C
NR_031668.1:n.44T>G (MIR1265)