Canonical Allele Identifier: CA2340161079
Gene: FTL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965242C= , CM000681.2:g.48965242C= GRCh38
NC_000019.9:g.49468499C= , CM000681.1:g.49468499C= GRCh37
NC_000019.8:g.54160311C= NCBI36
NG_008152.1:g.4934C=

Transcript Alleles

HGVS Amino-acid Change
XM_024451447.1:c.245C= XP_024307215.1:p.Pro82=