Canonical Allele Identifier: CA1105338
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 3095516
ClinVar RCV Id: RCV004386834
dbSNP Id: rs779294204
ExAC: 1:152281111 G / A
gnomAD v2: 1-152281111-G-A
gnomAD v4: 1-152308635-G-A
MyVariant Identifiers: chr1:g.152281111G>A (hg19) chr1:g.152308635G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308635G>A , CM000663.2:g.152308635G>A GRCh38
NC_000001.10:g.152281111G>A , CM000663.1:g.152281111G>A GRCh37
NC_000001.9:g.150547735G>A NCBI36
NG_016190.1:g.21569C>T , LRG_1028:g.21569C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.6251C>T MANE Select ENSP00000357789.1:p.Ser2084Phe
ENST00000368799.1:c.6251C>T ENSP00000357789.1:p.Ser2084Phe
NM_002016.1:c.6251C>T , LRG_1028t1:c.6251C>T NP_002007.1:p.Ser2084Phe
XM_011509329.1:c.6251C>T XP_011507631.1:p.Ser2084Phe
NM_002016.2:c.6251C>T MANE Select NP_002007.1:p.Ser2084Phe
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