Canonical Allele Identifier: CA633889287
Gene: FTL HGNC NCBI

Linked Data

dbSNP Id: rs765549925

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965760C>G , CM000681.2:g.48965760C>G GRCh38
NC_000019.9:g.49469017C>G , CM000681.1:g.49469017C>G GRCh37
NC_000019.8:g.54160829C>G NCBI36
NG_008152.1:g.5452C>G

Transcript Alleles

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