Canonical Allele Identifier: CA883052488
Gene: FTL HGNC NCBI

Linked Data

dbSNP Id: rs1398106673

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965752C>T , CM000681.2:g.48965752C>T GRCh38
NC_000019.9:g.49469009C>T , CM000681.1:g.49469009C>T GRCh37
NC_000019.8:g.54160821C>T NCBI36
NG_008152.1:g.5444C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000331825.11:c.103-18C>T MANE Select ENSP00000366525.2:n.103-18C>T
ENST00000331825.10:c.103-18C>T ENSP00000366525.2:n.103-18C>T
ENST00000622577.2:c.103-18C>T ENSP00000484043.1:n.103-18C>T
NM_000146.3:c.103-18C>T NP_000137.2:n.103-18C>T
XM_024451447.1:c.613-18C>T XP_024307215.1:n.613-18C>T
NM_000146.4:c.103-18C>T MANE Select NP_000137.2:n.103-18C>T