Canonical Allele Identifier: CA996657949
Gene: FTL HGNC NCBI

Linked Data

dbSNP Id: rs2038450249
gnomAD v3: 19-48966072-G-A
gnomAD v4: 19-48966072-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48966072G>A , CM000681.2:g.48966072G>A GRCh38
NC_000019.9:g.49469329G>A , CM000681.1:g.49469329G>A GRCh37
NC_000019.8:g.54161141G>A NCBI36
NG_008152.1:g.5764G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331825.11:c.249+156G>A MANE Select ENSP00000366525.2:n.249+156G>A
ENST00000331825.10:c.249+156G>A ENSP00000366525.2:n.249+156G>A
ENST00000622577.2:c.249+156G>A ENSP00000484043.1:n.249+156G>A
NM_000146.3:c.249+156G>A NP_000137.2:n.249+156G>A
XM_024451447.1:c.759+156G>A XP_024307215.1:n.759+156G>A
NM_000146.4:c.249+156G>A MANE Select NP_000137.2:n.249+156G>A
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