Canonical Allele Identifier: CA662078739
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1380040170
gnomAD v3: 10-14436409-C-G
gnomAD v4: 10-14436409-C-G
MyVariant Identifiers: chr10:g.14478408C>G (hg19) chr10:g.14436409C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436409C>G , CM000672.2:g.14436409C>G GRCh38
NC_000010.10:g.14478408C>G , CM000672.1:g.14478408C>G GRCh37
NC_000010.9:g.14518414C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25659G>C ENSP00000473870.1:n.-305+25659G>C
ENST00000493380.5:c.-82+25659G>C ENSP00000474863.1:n.-82+25659G>C
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