Canonical Allele Identifier: CA342074821
Gene: FLG HGNC NCBI

Linked Data

dbSNP Id: rs1383626477

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.152304991C>T , CM000663.2:g.152304991C>T GRCh38
NC_000001.10:g.152277467C>T , CM000663.1:g.152277467C>T GRCh37
NC_000001.9:g.150544091C>T NCBI36
NG_016190.1:g.25213G>A , LRG_1028:g.25213G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368799.2:c.9895G>A MANE Select ENSP00000357789.1:p.Gly3299Arg
ENST00000368799.1:c.9895G>A ENSP00000357789.1:p.Gly3299Arg
NM_002016.1:c.9895G>A , LRG_1028t1:c.9895G>A NP_002007.1:p.Gly3299Arg
XM_011509329.1:c.9108+787G>A XP_011507631.1:n.9108+787G>A
NM_002016.2:c.9895G>A MANE Select NP_002007.1:p.Gly3299Arg