Canonical Allele Identifier: CA309374807
Gene: FTL HGNC NCBI

Linked Data

dbSNP Id: rs980588240

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965260T>G , CM000681.2:g.48965260T>G GRCh38
NC_000019.9:g.49468517T>G , CM000681.1:g.49468517T>G GRCh37
NC_000019.8:g.54160329T>G NCBI36
NG_008152.1:g.4952T>G

Transcript Alleles

HGVS Amino-acid Change
XM_024451447.1:c.263T>G XP_024307215.1:p.Leu88Arg