Canonical Allele Identifier: CA1107178
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs138597668
ExAC: 1:152284932 T / C
gnomAD v2: 1-152284932-T-C
gnomAD v3: 1-152312456-T-C
gnomAD v4: 1-152312456-T-C
MyVariant Identifiers: chr1:g.152284932T>C (hg19) chr1:g.152312456T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152312456T>C , CM000663.2:g.152312456T>C GRCh38
NC_000001.10:g.152284932T>C , CM000663.1:g.152284932T>C GRCh37
NC_000001.9:g.150551556T>C NCBI36
NG_016190.1:g.17748A>G , LRG_1028:g.17748A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.2430A>G MANE Select ENSP00000357789.1:p.Thr810=
ENST00000368799.1:c.2430A>G ENSP00000357789.1:p.Thr810=
NM_002016.1:c.2430A>G , LRG_1028t1:c.2430A>G NP_002007.1:p.Thr810=
XM_011509329.1:c.2430A>G XP_011507631.1:p.Thr810=
NM_002016.2:c.2430A>G MANE Select NP_002007.1:p.Thr810=
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