Canonical Allele Identifier: CA2340161092
Gene: FTL HGNC NCBI

Linked Data

dbSNP Id: rs2038436870

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965267G>T , CM000681.2:g.48965267G>T GRCh38
NC_000019.9:g.49468524G>T , CM000681.1:g.49468524G>T GRCh37
NC_000019.8:g.54160336G>T NCBI36
NG_008152.1:g.4959G>T

Transcript Alleles

HGVS Amino-acid Change
XM_024451447.1:c.270G>T XP_024307215.1:p.Gly90=