Canonical Allele Identifier: CA309374795
Gene: FTL HGNC NCBI

Linked Data

dbSNP Id: rs1022608823
MyVariant Identifiers: chr19:g.49468494T>C (hg19) chr19:g.48965237T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965237T>C , CM000681.2:g.48965237T>C GRCh38
NC_000019.9:g.49468494T>C , CM000681.1:g.49468494T>C GRCh37
NC_000019.8:g.54160306T>C NCBI36
NG_008152.1:g.4929T>C

Transcript Alleles

HGVS Amino-acid Change
XM_024451447.1:c.240T>C XP_024307215.1:p.Ala80=
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