Canonical Allele Identifier: CA2340161126
Gene: FTL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965305C= , CM000681.2:g.48965305C= GRCh38
NC_000019.9:g.49468562C= , CM000681.1:g.49468562C= GRCh37
NC_000019.8:g.54160374C= NCBI36
NG_008152.1:g.4997C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.10:c.-203C= ENSP00000366525.2:n.-203C=
XM_024451447.1:c.308C= XP_024307215.1:p.Pro103=