Canonical Allele Identifier: CA1103522
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs765904861
ExAC: 1:152277231 C / T
gnomAD v2: 1-152277231-C-T
gnomAD v3: 1-152304755-C-T
gnomAD v4: 1-152304755-C-T
MyVariant Identifiers: chr1:g.152277231C>T (hg19) chr1:g.152304755C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304755C>T , CM000663.2:g.152304755C>T GRCh38
NC_000001.10:g.152277231C>T , CM000663.1:g.152277231C>T GRCh37
NC_000001.9:g.150543855C>T NCBI36
NG_016190.1:g.25449G>A , LRG_1028:g.25449G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.10131G>A MANE Select ENSP00000357789.1:p.Gly3377=
ENST00000368799.1:c.10131G>A ENSP00000357789.1:p.Gly3377=
NM_002016.1:c.10131G>A , LRG_1028t1:c.10131G>A NP_002007.1:p.Gly3377=
XM_011509329.1:c.9109-922G>A XP_011507631.1:n.9109-922G>A
NM_002016.2:c.10131G>A MANE Select NP_002007.1:p.Gly3377=
Search 100 bp 5'
Search 100 bp 3'