Canonical Allele Identifier: CA2586287913
Gene: FTL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965262C>A , CM000681.2:g.48965262C>A GRCh38
NC_000019.9:g.49468519C>A , CM000681.1:g.49468519C>A GRCh37
NC_000019.8:g.54160331C>A NCBI36
NG_008152.1:g.4954C>A

Transcript Alleles

HGVS Amino-acid Change
XM_024451447.1:c.265C>A XP_024307215.1:p.Arg89=