Canonical Allele Identifier: CA468386371
Gene: FRMD4A HGNC NCBI
MIR1265 HGNC NCBI

Linked Data

dbSNP Id: rs2130667445
gnomAD v4: 10-14436648-A-G
MyVariant Identifiers: chr10:g.14478647A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436648A>G , CM000672.2:g.14436648A>G GRCh38
NC_000010.10:g.14478647A>G , CM000672.1:g.14478647A>G GRCh37
NC_000010.9:g.14518653A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25420T>C (FRMD4A) ENSP00000473870.1:n.-305+25420T>C
ENST00000493380.5:c.-82+25420T>C (FRMD4A) ENSP00000474863.1:n.-82+25420T>C
NR_031668.1:n.73A>G (MIR1265)
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