Canonical Allele Identifier: CA1892118485
Gene: FRMD4A HGNC NCBI

Linked Data

dbSNP Id: rs1844563168
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14436959C>T , CM000672.2:g.14436959C>T GRCh38
NC_000010.10:g.14478958C>T , CM000672.1:g.14478958C>T GRCh37
NC_000010.9:g.14518964C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475141.2:c.-305+25109G>A ENSP00000473870.1:n.-305+25109G>A
ENST00000493380.5:c.-82+25109G>A ENSP00000474863.1:n.-82+25109G>A
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