Canonical Allele Identifier: CA468386407
Gene: FRMD4A HGNC NCBI
MIR1265 HGNC NCBI

Linked Data

dbSNP Id: rs1446688650
gnomAD v2: 10-14478659-A-G
gnomAD v3: 10-14436660-A-G
gnomAD v4: 10-14436660-A-G
MyVariant Identifiers: chr10:g.14478659A>G (hg19) chr10:g.14436660A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436660A>G , CM000672.2:g.14436660A>G GRCh38
NC_000010.10:g.14478659A>G , CM000672.1:g.14478659A>G GRCh37
NC_000010.9:g.14518665A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25408T>C (FRMD4A) ENSP00000473870.1:n.-305+25408T>C
ENST00000493380.5:c.-82+25408T>C (FRMD4A) ENSP00000474863.1:n.-82+25408T>C
NR_031668.1:n.85A>G (MIR1265)
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