Canonical Allele Identifier: CA2340161111
Gene: FTL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965294T= , CM000681.2:g.48965294T= GRCh38
NC_000019.9:g.49468551T= , CM000681.1:g.49468551T= GRCh37
NC_000019.8:g.54160363T= NCBI36
NG_008152.1:g.4986T=

Transcript Alleles

HGVS Amino-acid Change
XM_024451447.1:c.297T= XP_024307215.1:p.Pro99=