Canonical Allele Identifier: CA1104875
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2639271
ClinVar RCV Id: RCV003408965
dbSNP Id: rs773927647
ExAC: 1:152280198 C / T
gnomAD v2: 1-152280198-C-T
gnomAD v3: 1-152307722-C-T
gnomAD v4: 1-152307722-C-T
MyVariant Identifiers: chr1:g.152280198C>T (hg19) chr1:g.152280198_152280199delinsTT (hg19) chr1:g.152307722C>T (hg38) chr1:g.152307722_152307723delinsTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152307722C>T , CM000663.2:g.152307722C>T GRCh38
NC_000001.10:g.152280198C>T , CM000663.1:g.152280198C>T GRCh37
NC_000001.9:g.150546822C>T NCBI36
NG_016190.1:g.22482G>A , LRG_1028:g.22482G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.7164G>A MANE Select ENSP00000357789.1:p.Gln2388=
ENST00000368799.1:c.7164G>A ENSP00000357789.1:p.Gln2388=
NM_002016.1:c.7164G>A , LRG_1028t1:c.7164G>A NP_002007.1:p.Gln2388=
XM_011509329.1:c.7164G>A XP_011507631.1:p.Gln2388=
NM_002016.2:c.7164G>A MANE Select NP_002007.1:p.Gln2388=
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