Canonical Allele Identifier: CA592244856
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs553492855
gnomAD v2: 10-14478684-G-C
gnomAD v3: 10-14436685-G-C
gnomAD v4: 10-14436685-G-C
MyVariant Identifiers: chr10:g.14478684G>C (hg19) chr10:g.14436685G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436685G>C , CM000672.2:g.14436685G>C GRCh38
NC_000010.10:g.14478684G>C , CM000672.1:g.14478684G>C GRCh37
NC_000010.9:g.14518690G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25383C>G ENSP00000473870.1:n.-305+25383C>G
ENST00000493380.5:c.-82+25383C>G ENSP00000474863.1:n.-82+25383C>G
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