Canonical Allele Identifier: CA2586287911
Gene: FTL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965259C>T , CM000681.2:g.48965259C>T GRCh38
NC_000019.9:g.49468516C>T , CM000681.1:g.49468516C>T GRCh37
NC_000019.8:g.54160328C>T NCBI36
NG_008152.1:g.4951C>T

Transcript Alleles

HGVS Amino-acid Change
XM_024451447.1:c.262C>T XP_024307215.1:p.Leu88Phe