Canonical Allele Identifier: CA1103646
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs749472491
ExAC: 1:152277508 C / A
gnomAD v2: 1-152277508-C-A
gnomAD v4: 1-152305032-C-A
MyVariant Identifiers: chr1:g.152277508C>A (hg19) chr1:g.152305032C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152305032C>A , CM000663.2:g.152305032C>A GRCh38
NC_000001.10:g.152277508C>A , CM000663.1:g.152277508C>A GRCh37
NC_000001.9:g.150544132C>A NCBI36
NG_016190.1:g.25172G>T , LRG_1028:g.25172G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9854G>T MANE Select ENSP00000357789.1:p.Gly3285Val
ENST00000368799.1:c.9854G>T ENSP00000357789.1:p.Gly3285Val
NM_002016.1:c.9854G>T , LRG_1028t1:c.9854G>T NP_002007.1:p.Gly3285Val
XM_011509329.1:c.9108+746G>T XP_011507631.1:n.9108+746G>T
NM_002016.2:c.9854G>T MANE Select NP_002007.1:p.Gly3285Val
Search 100 bp 5'
Search 100 bp 3'