Canonical Allele Identifier: CA2586287932
Gene: FTL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965281A>G , CM000681.2:g.48965281A>G GRCh38
NC_000019.9:g.49468538A>G , CM000681.1:g.49468538A>G GRCh37
NC_000019.8:g.54160350A>G NCBI36
NG_008152.1:g.4973A>G

Transcript Alleles

HGVS Amino-acid Change
XM_024451447.1:c.284A>G XP_024307215.1:p.Lys95Arg