Canonical Allele Identifier: CA2586287922
Gene: FTL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965269C>A , CM000681.2:g.48965269C>A GRCh38
NC_000019.9:g.49468526C>A , CM000681.1:g.49468526C>A GRCh37
NC_000019.8:g.54160338C>A NCBI36
NG_008152.1:g.4961C>A

Transcript Alleles

HGVS Amino-acid Change
XM_024451447.1:c.272C>A XP_024307215.1:p.Pro91Gln