Canonical Allele Identifier: CA1103592
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs766141730
ExAC: 1:152277365 A / T
gnomAD v2: 1-152277365-A-T
gnomAD v4: 1-152304889-A-T
MyVariant Identifiers: chr1:g.152277365A>T (hg19) chr1:g.152304889A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304889A>T , CM000663.2:g.152304889A>T GRCh38
NC_000001.10:g.152277365A>T , CM000663.1:g.152277365A>T GRCh37
NC_000001.9:g.150543989A>T NCBI36
NG_016190.1:g.25315T>A , LRG_1028:g.25315T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9997T>A MANE Select ENSP00000357789.1:p.Trp3333Arg
ENST00000368799.1:c.9997T>A ENSP00000357789.1:p.Trp3333Arg
NM_002016.1:c.9997T>A , LRG_1028t1:c.9997T>A NP_002007.1:p.Trp3333Arg
XM_011509329.1:c.9108+889T>A XP_011507631.1:n.9108+889T>A
NM_002016.2:c.9997T>A MANE Select NP_002007.1:p.Trp3333Arg
Search 100 bp 5'
Search 100 bp 3'