Canonical Allele Identifier: CA203745857
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs150210091
gnomAD v2: 10-14478406-G-A
gnomAD v3: 10-14436407-G-A
gnomAD v4: 10-14436407-G-A
MyVariant Identifiers: chr10:g.14478406G>A (hg19) chr10:g.14436407G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436407G>A , CM000672.2:g.14436407G>A GRCh38
NC_000010.10:g.14478406G>A , CM000672.1:g.14478406G>A GRCh37
NC_000010.9:g.14518412G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25661C>T ENSP00000473870.1:n.-305+25661C>T
ENST00000493380.5:c.-82+25661C>T ENSP00000474863.1:n.-82+25661C>T
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