Canonical Allele Identifier: CA2586287923
Gene: FTL HGNC NCBI

Linked Data

dbSNP Id: rs2122429219

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965270G>A , CM000681.2:g.48965270G>A GRCh38
NC_000019.9:g.49468527G>A , CM000681.1:g.49468527G>A GRCh37
NC_000019.8:g.54160339G>A NCBI36
NG_008152.1:g.4962G>A

Transcript Alleles

HGVS Amino-acid Change
XM_024451447.1:c.273G>A XP_024307215.1:p.Pro91=