Canonical Allele Identifier: CA2586287897
Gene: FTL HGNC NCBI

Linked Data

gnomAD v4: 19-48965246-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48965246C>G , CM000681.2:g.48965246C>G GRCh38
NC_000019.9:g.49468503C>G , CM000681.1:g.49468503C>G GRCh37
NC_000019.8:g.54160315C>G NCBI36
NG_008152.1:g.4938C>G

Transcript Alleles

HGVS Amino-acid Change
XM_024451447.1:c.249C>G XP_024307215.1:p.Pro83=
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