Canonical Allele Identifier: CA5415006

Gene: FRMD4A MIR1265

Linked Data

• dbSNP Id: rs149384303
• ExAC: 10:14478576 T / C
• gnomAD v2: 10-14478576-T-C
• gnomAD v3: 10-14436577-T-C
• gnomAD v4: 10-14436577-T-C
• MyVariant Identifiers: chr10:g.14478576T>C (hg19) ; chr10:g.14436577T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14436577T>C , CM000672.2:g.14436577T>C	GRCh38
NC_000010.10:g.14478576T>C , CM000672.1:g.14478576T>C	GRCh37
NC_000010.9:g.14518582T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000475141.2:c.-305+25491A>G (FRMD4A)	ENSP00000473870.1:n.-305+25491A>G
ENST00000493380.5:c.-82+25491A>G (FRMD4A)	ENSP00000474863.1:n.-82+25491A>G
NR_031668.1:n.2T>C (MIR1265)