Canonical Allele Identifier: CA1105526
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1272269
ClinVar RCV Id: RCV001686425
dbSNP Id: rs111661820
ExAC: 1:152281466 C / T
gnomAD v2: 1-152281466-C-T
gnomAD v3: 1-152308990-C-T
gnomAD v4: 1-152308990-C-T
MyVariant Identifiers: chr1:g.152281466C>T (hg19) chr1:g.152308990C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152308990C>T , CM000663.2:g.152308990C>T GRCh38
NC_000001.10:g.152281466C>T , CM000663.1:g.152281466C>T GRCh37
NC_000001.9:g.150548090C>T NCBI36
NG_016190.1:g.21214G>A , LRG_1028:g.21214G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.5896G>A MANE Select ENSP00000357789.1:p.Gly1966Ser
ENST00000368799.1:c.5896G>A ENSP00000357789.1:p.Gly1966Ser
NM_002016.1:c.5896G>A , LRG_1028t1:c.5896G>A NP_002007.1:p.Gly1966Ser
XM_011509329.1:c.5896G>A XP_011507631.1:p.Gly1966Ser
NM_002016.2:c.5896G>A MANE Select NP_002007.1:p.Gly1966Ser
Search 100 bp 5'
Search 100 bp 3'