Canonical Allele Identifier: CA1105597
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs750443245
ExAC: 1:152281587 C / T
gnomAD v2: 1-152281587-C-T
MyVariant Identifiers: chr1:g.152281587C>T (hg19) chr1:g.152309111C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152309111C>T , CM000663.2:g.152309111C>T GRCh38
NC_000001.10:g.152281587C>T , CM000663.1:g.152281587C>T GRCh37
NC_000001.9:g.150548211C>T NCBI36
NG_016190.1:g.21093G>A , LRG_1028:g.21093G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5775G>A MANE Select ENSP00000357789.1:p.Gln1925=
ENST00000368799.1:c.5775G>A ENSP00000357789.1:p.Gln1925=
NM_002016.1:c.5775G>A , LRG_1028t1:c.5775G>A NP_002007.1:p.Gln1925=
XM_011509329.1:c.5775G>A XP_011507631.1:p.Gln1925=
NM_002016.2:c.5775G>A MANE Select NP_002007.1:p.Gln1925=
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