Canonical Allele Identifier: CA662078720
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1202636252
MyVariant Identifiers: chr10:g.14478393A>C (hg19) chr10:g.14436394A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436394A>C , CM000672.2:g.14436394A>C GRCh38
NC_000010.10:g.14478393A>C , CM000672.1:g.14478393A>C GRCh37
NC_000010.9:g.14518399A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475141.2:c.-305+25674T>G ENSP00000473870.1:n.-305+25674T>G
ENST00000493380.5:c.-82+25674T>G ENSP00000474863.1:n.-82+25674T>G
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